Canonical Allele Identifier: CA395410074

Gene: ATXN2L

Linked Data

• gnomAD v4: 16-28836140-G-T
• MyVariant Identifiers: chr16:g.28847461G>T (hg19) ; chr16:g.28836140G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28836140G>T , CM000678.2:g.28836140G>T	GRCh38
NC_000016.9:g.28847461G>T , CM000678.1:g.28847461G>T	GRCh37
NC_000016.8:g.28754962G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336783.9:c.3103G>T MANE Select	ENSP00000338718.4:p.Ala1035Ser
ENST00000325215.10:c.3103G>T	ENSP00000315650.6:p.Ala1035Ser
ENST00000336783.8:c.3103G>T	ENSP00000338718.4:p.Ala1035Ser
ENST00000340394.12:c.3085+18G>T	ENSP00000341459.8:n.3085+18G>T
ENST00000382686.8:c.3085+18G>T	ENSP00000372133.4:n.3085+18G>T
ENST00000395547.6:c.3103G>T	ENSP00000378917.2:p.Ala1035Ser
ENST00000562583.5:c.1078G>T	ENSP00000456162.2:p.Ala360Ser
ENST00000563314.5:n.3477G>T
ENST00000564162.1:c.280+18G>T	ENSP00000455427.1:n.280+18G>T
ENST00000564304.5:c.3121G>T	ENSP00000457613.1:p.Ala1041Ser
ENST00000565971.5:c.2167G>T	ENSP00000457599.1:n.2167G>T
ENST00000566007.5:c.354+18G>T
ENST00000566946.5:c.1081G>T	ENSP00000454757.1:p.Ala361Ser
ENST00000570200.5:c.3103G>T	ENSP00000454516.1:p.Ala1035Ser
NM_001308230.1:c.3121G>T	NP_001295159.1:p.Ala1041Ser
NM_007245.3:c.3103G>T	NP_009176.2:p.Ala1035Ser
NM_017492.3:c.3103G>T	NP_059867.3:p.Ala1035Ser
NM_145714.2:c.3103G>T	NP_663760.1:p.Ala1035Ser
NM_148414.2:c.3103G>T	NP_680780.1:p.Ala1035Ser
NM_148415.2:c.3085+18G>T	NP_680781.1:n.3085+18G>T
NM_148416.2:c.3085+18G>T	NP_680782.1:n.3085+18G>T
XM_005255061.1:c.3124G>T	XP_005255118.1:p.Ala1042Ser
XM_005255062.1:c.3124G>T	XP_005255119.1:p.Ala1042Ser
XM_005255063.2:c.3124G>T	XP_005255120.1:p.Ala1042Ser
XM_005255064.1:c.3121G>T	XP_005255121.1:p.Ala1041Ser
XM_005255065.1:c.3106G>T	XP_005255122.1:p.Ala1036Ser
XM_005255066.1:c.3103G>T	XP_005255123.1:p.Ala1035Ser
XM_005255067.1:c.3106+18G>T	XP_005255124.1:n.3106+18G>T
XM_005255068.1:c.3106+18G>T	XP_005255125.1:n.3106+18G>T
XM_005255069.1:c.3124G>T	XP_005255126.1:p.Ala1042Ser
XM_005255070.1:c.3124G>T	XP_005255127.1:p.Ala1042Ser
XM_005255071.1:c.3124G>T	XP_005255128.1:p.Ala1042Ser
XM_005255074.1:c.3106+18G>T	XP_005255131.1:n.3106+18G>T
XM_005255075.1:c.3106+18G>T	XP_005255132.1:n.3106+18G>T
XM_005255076.1:c.3103+18G>T	XP_005255133.1:n.3103+18G>T
XM_005255077.1:c.2944G>T	XP_005255134.1:p.Ala982Ser
XM_006721007.1:c.3052G>T	XP_006721070.1:p.Ala1018Ser
XM_006721008.1:c.3034G>T	XP_006721071.1:p.Ala1012Ser
XM_006721009.1:c.3124G>T	XP_006721072.1:p.Ala1042Ser
XM_006721010.2:c.3124G>T	XP_006721073.1:p.Ala1042Ser
XM_006721011.1:c.3106+18G>T	XP_006721074.1:n.3106+18G>T
XM_006721012.2:c.3106+18G>T	XP_006721075.1:n.3106+18G>T
XM_006721013.2:c.3106+18G>T	XP_006721076.1:n.3106+18G>T
XM_011545719.1:c.3124G>T	XP_011544021.1:p.Ala1042Ser
XM_011545720.1:c.3124G>T	XP_011544022.1:p.Ala1042Ser
XM_011545721.1:c.3106+18G>T	XP_011544023.1:n.3106+18G>T
XM_011545722.1:c.2758G>T	XP_011544024.1:p.Ala920Ser
XR_243256.1:n.3333G>T
XM_005255063.4:c.3124G>T	XP_005255120.1:p.Ala1042Ser
XM_006721012.4:c.3106+18G>T	XP_006721075.1:n.3106+18G>T
XM_011545719.2:c.3124G>T	XP_011544021.1:p.Ala1042Ser
XM_017022891.1:c.2926G>T	XP_016878380.1:p.Ala976Ser
XM_017022892.1:c.2740G>T	XP_016878381.1:p.Ala914Ser
XR_001751820.1:n.3336G>T
NM_001308230.2:c.3121G>T	NP_001295159.1:p.Ala1041Ser
NM_001387166.1:c.3121G>T	NP_001374095.1:p.Ala1041Ser
NM_001387167.1:c.3103G>T	NP_001374096.1:p.Ala1035Ser
NM_001387168.1:c.3103G>T	NP_001374097.1:p.Ala1035Ser
NM_001387169.1:c.3103+18G>T	NP_001374098.1:n.3103+18G>T
NM_001387170.1:c.3103+18G>T	NP_001374099.1:n.3103+18G>T
NM_001387171.1:c.3124G>T	NP_001374100.1:p.Ala1042Ser
NM_001387172.1:c.3121G>T	NP_001374101.1:p.Ala1041Ser
NM_001387173.1:c.3088+18G>T	NP_001374102.1:n.3088+18G>T
NM_001387174.1:c.3085+18G>T	NP_001374103.1:n.3085+18G>T
NM_001387175.1:c.3085+18G>T	NP_001374104.1:n.3085+18G>T
NM_001387176.1:c.3085+18G>T	NP_001374105.1:n.3085+18G>T
NM_001387177.1:c.3085+18G>T	NP_001374106.1:n.3085+18G>T
NM_001387178.1:c.3106G>T	NP_001374107.1:p.Ala1036Ser
NM_001387179.1:c.3031G>T	NP_001374108.1:p.Ala1011Ser
NM_001387180.1:c.3097G>T	NP_001374109.1:p.Ala1033Ser
NM_001387181.1:c.3124G>T	NP_001374110.1:p.Ala1042Ser
NM_001387182.1:c.3121G>T	NP_001374111.1:p.Ala1041Ser
NM_001387183.1:c.3106G>T	NP_001374112.1:p.Ala1036Ser
NM_001387184.1:c.3106G>T	NP_001374113.1:p.Ala1036Ser
NM_001387185.1:c.3013+18G>T	NP_001374114.1:n.3013+18G>T
NM_001387186.1:c.3034G>T	NP_001374115.1:p.Ala1012Ser
NM_001387187.1:c.3034G>T	NP_001374116.1:p.Ala1012Ser
NM_001387188.1:c.3031G>T	NP_001374117.1:p.Ala1011Ser
NM_001387189.1:c.3103+18G>T	NP_001374118.1:n.3103+18G>T
NM_001387190.1:c.3103+18G>T	NP_001374119.1:n.3103+18G>T
NM_001387191.1:c.3088+18G>T	NP_001374120.1:n.3088+18G>T
NM_001387192.1:c.3088+18G>T	NP_001374121.1:n.3088+18G>T
NM_001387193.1:c.3103+18G>T	NP_001374122.1:n.3103+18G>T
NM_001387194.1:c.3088+18G>T	NP_001374123.1:n.3088+18G>T
NM_001387195.1:c.3085+18G>T	NP_001374124.1:n.3085+18G>T
NM_001387196.1:c.3085+18G>T	NP_001374125.1:n.3085+18G>T
NM_001387197.1:c.3049G>T	NP_001374126.1:p.Ala1017Ser
NM_001387198.1:c.3085+18G>T	NP_001374127.1:n.3085+18G>T
NM_001387199.1:c.3016+18G>T	NP_001374128.1:n.3016+18G>T
NM_001387200.1:c.3031+18G>T	NP_001374129.1:n.3031+18G>T
NM_001387202.1:c.3013+18G>T	NP_001374131.1:n.3013+18G>T
NM_001387203.1:c.2914G>T	NP_001374132.1:p.Ala972Ser
NM_001387204.1:c.2913G>T	NP_001374133.1:p.Arg971Ser
NM_007245.4:c.3103G>T MANE Select	NP_009176.2:p.Ala1035Ser
NM_017492.4:c.3103G>T	NP_059867.3:p.Ala1035Ser
NM_145714.3:c.3103G>T	NP_663760.1:p.Ala1035Ser
NM_148414.3:c.3103G>T	NP_680780.1:p.Ala1035Ser
NM_148415.3:c.3085+18G>T	NP_680781.1:n.3085+18G>T
NM_148416.3:c.3085+18G>T	NP_680782.1:n.3085+18G>T