Canonical Allele Identifier: CA395410033

Gene: ATXN2L

Linked Data

• MyVariant Identifiers: chr16:g.28847452C>A (hg19) ; chr16:g.28836131C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28836131C>A , CM000678.2:g.28836131C>A	GRCh38
NC_000016.9:g.28847452C>A , CM000678.1:g.28847452C>A	GRCh37
NC_000016.8:g.28754953C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336783.9:c.3094C>A MANE Select	ENSP00000338718.4:p.Pro1032Thr
ENST00000325215.10:c.3094C>A	ENSP00000315650.6:p.Pro1032Thr
ENST00000336783.8:c.3094C>A	ENSP00000338718.4:p.Pro1032Thr
ENST00000340394.12:c.3085+9C>A	ENSP00000341459.8:n.3085+9C>A
ENST00000382686.8:c.3085+9C>A	ENSP00000372133.4:n.3085+9C>A
ENST00000395547.6:c.3094C>A	ENSP00000378917.2:p.Pro1032Thr
ENST00000562583.5:c.1069C>A	ENSP00000456162.2:p.Pro357Thr
ENST00000563314.5:n.3468C>A
ENST00000564162.1:c.280+9C>A	ENSP00000455427.1:n.280+9C>A
ENST00000564304.5:c.3112C>A	ENSP00000457613.1:p.Pro1038Thr
ENST00000565971.5:c.2158C>A	ENSP00000457599.1:n.2158C>A
ENST00000566007.5:c.354+9C>A
ENST00000566946.5:c.1072C>A	ENSP00000454757.1:p.Pro358Thr
ENST00000570200.5:c.3094C>A	ENSP00000454516.1:p.Pro1032Thr
NM_001308230.1:c.3112C>A	NP_001295159.1:p.Pro1038Thr
NM_007245.3:c.3094C>A	NP_009176.2:p.Pro1032Thr
NM_017492.3:c.3094C>A	NP_059867.3:p.Pro1032Thr
NM_145714.2:c.3094C>A	NP_663760.1:p.Pro1032Thr
NM_148414.2:c.3094C>A	NP_680780.1:p.Pro1032Thr
NM_148415.2:c.3085+9C>A	NP_680781.1:n.3085+9C>A
NM_148416.2:c.3085+9C>A	NP_680782.1:n.3085+9C>A
XM_005255061.1:c.3115C>A	XP_005255118.1:p.Pro1039Thr
XM_005255062.1:c.3115C>A	XP_005255119.1:p.Pro1039Thr
XM_005255063.2:c.3115C>A	XP_005255120.1:p.Pro1039Thr
XM_005255064.1:c.3112C>A	XP_005255121.1:p.Pro1038Thr
XM_005255065.1:c.3097C>A	XP_005255122.1:p.Pro1033Thr
XM_005255066.1:c.3094C>A	XP_005255123.1:p.Pro1032Thr
XM_005255067.1:c.3106+9C>A	XP_005255124.1:n.3106+9C>A
XM_005255068.1:c.3106+9C>A	XP_005255125.1:n.3106+9C>A
XM_005255069.1:c.3115C>A	XP_005255126.1:p.Pro1039Thr
XM_005255070.1:c.3115C>A	XP_005255127.1:p.Pro1039Thr
XM_005255071.1:c.3115C>A	XP_005255128.1:p.Pro1039Thr
XM_005255074.1:c.3106+9C>A	XP_005255131.1:n.3106+9C>A
XM_005255075.1:c.3106+9C>A	XP_005255132.1:n.3106+9C>A
XM_005255076.1:c.3103+9C>A	XP_005255133.1:n.3103+9C>A
XM_005255077.1:c.2935C>A	XP_005255134.1:p.Pro979Thr
XM_006721007.1:c.3043C>A	XP_006721070.1:p.Pro1015Thr
XM_006721008.1:c.3025C>A	XP_006721071.1:p.Pro1009Thr
XM_006721009.1:c.3115C>A	XP_006721072.1:p.Pro1039Thr
XM_006721010.2:c.3115C>A	XP_006721073.1:p.Pro1039Thr
XM_006721011.1:c.3106+9C>A	XP_006721074.1:n.3106+9C>A
XM_006721012.2:c.3106+9C>A	XP_006721075.1:n.3106+9C>A
XM_006721013.2:c.3106+9C>A	XP_006721076.1:n.3106+9C>A
XM_011545719.1:c.3115C>A	XP_011544021.1:p.Pro1039Thr
XM_011545720.1:c.3115C>A	XP_011544022.1:p.Pro1039Thr
XM_011545721.1:c.3106+9C>A	XP_011544023.1:n.3106+9C>A
XM_011545722.1:c.2749C>A	XP_011544024.1:p.Pro917Thr
XR_243256.1:n.3324C>A
XM_005255063.4:c.3115C>A	XP_005255120.1:p.Pro1039Thr
XM_006721012.4:c.3106+9C>A	XP_006721075.1:n.3106+9C>A
XM_011545719.2:c.3115C>A	XP_011544021.1:p.Pro1039Thr
XM_017022891.1:c.2917C>A	XP_016878380.1:p.Pro973Thr
XM_017022892.1:c.2731C>A	XP_016878381.1:p.Pro911Thr
XR_001751820.1:n.3327C>A
NM_001308230.2:c.3112C>A	NP_001295159.1:p.Pro1038Thr
NM_001387166.1:c.3112C>A	NP_001374095.1:p.Pro1038Thr
NM_001387167.1:c.3094C>A	NP_001374096.1:p.Pro1032Thr
NM_001387168.1:c.3094C>A	NP_001374097.1:p.Pro1032Thr
NM_001387169.1:c.3103+9C>A	NP_001374098.1:n.3103+9C>A
NM_001387170.1:c.3103+9C>A	NP_001374099.1:n.3103+9C>A
NM_001387171.1:c.3115C>A	NP_001374100.1:p.Pro1039Thr
NM_001387172.1:c.3112C>A	NP_001374101.1:p.Pro1038Thr
NM_001387173.1:c.3088+9C>A	NP_001374102.1:n.3088+9C>A
NM_001387174.1:c.3085+9C>A	NP_001374103.1:n.3085+9C>A
NM_001387175.1:c.3085+9C>A	NP_001374104.1:n.3085+9C>A
NM_001387176.1:c.3085+9C>A	NP_001374105.1:n.3085+9C>A
NM_001387177.1:c.3085+9C>A	NP_001374106.1:n.3085+9C>A
NM_001387178.1:c.3097C>A	NP_001374107.1:p.Pro1033Thr
NM_001387179.1:c.3022C>A	NP_001374108.1:p.Pro1008Thr
NM_001387180.1:c.3088C>A	NP_001374109.1:p.Pro1030Thr
NM_001387181.1:c.3115C>A	NP_001374110.1:p.Pro1039Thr
NM_001387182.1:c.3112C>A	NP_001374111.1:p.Pro1038Thr
NM_001387183.1:c.3097C>A	NP_001374112.1:p.Pro1033Thr
NM_001387184.1:c.3097C>A	NP_001374113.1:p.Pro1033Thr
NM_001387185.1:c.3013+9C>A	NP_001374114.1:n.3013+9C>A
NM_001387186.1:c.3025C>A	NP_001374115.1:p.Pro1009Thr
NM_001387187.1:c.3025C>A	NP_001374116.1:p.Pro1009Thr
NM_001387188.1:c.3022C>A	NP_001374117.1:p.Pro1008Thr
NM_001387189.1:c.3103+9C>A	NP_001374118.1:n.3103+9C>A
NM_001387190.1:c.3103+9C>A	NP_001374119.1:n.3103+9C>A
NM_001387191.1:c.3088+9C>A	NP_001374120.1:n.3088+9C>A
NM_001387192.1:c.3088+9C>A	NP_001374121.1:n.3088+9C>A
NM_001387193.1:c.3103+9C>A	NP_001374122.1:n.3103+9C>A
NM_001387194.1:c.3088+9C>A	NP_001374123.1:n.3088+9C>A
NM_001387195.1:c.3085+9C>A	NP_001374124.1:n.3085+9C>A
NM_001387196.1:c.3085+9C>A	NP_001374125.1:n.3085+9C>A
NM_001387197.1:c.3040C>A	NP_001374126.1:p.Pro1014Thr
NM_001387198.1:c.3085+9C>A	NP_001374127.1:n.3085+9C>A
NM_001387199.1:c.3016+9C>A	NP_001374128.1:n.3016+9C>A
NM_001387200.1:c.3031+9C>A	NP_001374129.1:n.3031+9C>A
NM_001387202.1:c.3013+9C>A	NP_001374131.1:n.3013+9C>A
NM_001387203.1:c.2905C>A	NP_001374132.1:p.Pro969Thr
NM_001387204.1:c.2904C>A	NP_001374133.1:p.Ser968Arg
NM_007245.4:c.3094C>A MANE Select	NP_009176.2:p.Pro1032Thr
NM_017492.4:c.3094C>A	NP_059867.3:p.Pro1032Thr
NM_145714.3:c.3094C>A	NP_663760.1:p.Pro1032Thr
NM_148414.3:c.3094C>A	NP_680780.1:p.Pro1032Thr
NM_148415.3:c.3085+9C>A	NP_680781.1:n.3085+9C>A
NM_148416.3:c.3085+9C>A	NP_680782.1:n.3085+9C>A