Canonical Allele Identifier: CA411648771

Gene: ADSL

Linked Data

• gnomAD v4: 22-40365052-A-G
• MyVariant Identifiers: chr22:g.40761056A>G (hg19) ; chr22:g.40365052A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40365052A>G , CM000684.2:g.40365052A>G	GRCh38
NC_000022.10:g.40761056A>G , CM000684.1:g.40761056A>G	GRCh37
NC_000022.9:g.39091002A>G	NCBI36
NG_007993.1:g.23553A>G
NG_007993.2:g.23553A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*758A>G	ENSP00000485462.2:n.*758A>G
ENST00000623287.4:c.*789A>G	ENSP00000485437.1:n.*789A>G
ENST00000623632.4:c.1055A>G	ENSP00000485288.2:p.Gln352Arg
ENST00000625194.4:c.1406A>G	ENSP00000485289.2:p.Gln469Arg
ENST00000636433.1:n.1386A>G
ENST00000636714.1:c.1364A>G	ENSP00000490946.1:p.Gln455Arg
ENST00000637666.2:c.1191+687A>G	ENSP00000489696.2:n.1191+687A>G
ENST00000637669.1:c.1364A>G	ENSP00000489728.1:p.Gln455Arg
ENST00000639722.1:c.*1060A>G	ENSP00000492828.1:n.*1060A>G
ENST00000674592.1:n.2878A>G
ENST00000675622.1:n.4431A>G
ENST00000679609.1:c.*974A>G	ENSP00000506592.1:n.*974A>G
ENST00000679656.1:n.2049A>G
ENST00000679723.1:c.1319A>G	ENSP00000505155.1:p.Gln440Arg
ENST00000679845.1:n.1672A>G
ENST00000679904.1:n.1760A>G
ENST00000680378.1:c.1451A>G	ENSP00000505556.1:p.Gln484Arg
ENST00000680444.1:c.*727A>G	ENSP00000505298.1:n.*727A>G
ENST00000680978.1:c.1364A>G	ENSP00000505244.1:p.Gln455Arg
ENST00000681003.1:n.827A>G
ENST00000681159.1:n.2768A>G
ENST00000216194.11:c.1406A>G	ENSP00000216194.8:p.Gln469Arg
ENST00000342312.9:c.1191+687A>G	ENSP00000341429.6:n.1191+687A>G
ENST00000423176.6:c.91A>G
ENST00000498234.2:c.22A>G
ENST00000623063.3:c.1364A>G MANE Select	ENSP00000485525.1:p.Gln455Arg
ENST00000623387.1:n.495A>G
ENST00000623869.3:c.95A>G	ENSP00000485211.1:p.Gln32Arg
ENST00000624027.1:c.91A>G
ENST00000625194.3:c.993A>G
NM_000026.2:c.1364A>G	NP_000017.1:p.Gln455Arg
NM_001123378.1:c.1191+687A>G	NP_001116850.1:n.1191+687A>G
XM_011529976.1:c.1364A>G	XP_011528278.1:p.Gln455Arg
XM_011529977.1:c.1364A>G	XP_011528279.1:p.Gln455Arg
XM_011529978.1:c.1191+687A>G	XP_011528280.1:n.1191+687A>G
XM_011529979.1:c.1364A>G	XP_011528281.1:p.Gln455Arg
XM_011529980.1:c.1191+687A>G	XP_011528282.1:n.1191+687A>G
XM_011529981.1:c.899A>G	XP_011528283.1:p.Gln300Arg
XM_011529982.1:c.533A>G	XP_011528284.1:p.Gln178Arg
XR_937824.1:n.1454A>G
XR_937825.1:n.1281+687A>G
NM_000026.3:c.1364A>G	NP_000017.1:p.Gln455Arg
NM_001123378.2:c.1191+687A>G	NP_001116850.1:n.1191+687A>G
NM_001317923.1:c.1172A>G	NP_001304852.1:p.Gln391Arg
NM_001363840.1:c.1364A>G	NP_001350769.1:p.Gln455Arg
NR_134256.1:n.1454A>G
XM_011529977.3:c.1364A>G	XP_011528279.1:p.Gln455Arg
XM_011529980.3:c.1191+687A>G	XP_011528282.1:n.1191+687A>G
XM_017028636.1:c.1319A>G	XP_016884125.1:p.Gln440Arg
XM_017028637.1:c.1319A>G	XP_016884126.1:p.Gln440Arg
XM_017028638.1:c.899A>G	XP_016884127.1:p.Gln300Arg
XM_017028639.2:c.899A>G	XP_016884128.1:p.Gln300Arg
XM_017028640.1:c.533A>G	XP_016884129.1:p.Gln178Arg
XM_024452166.1:c.1146+687A>G	XP_024307934.1:n.1146+687A>G
XR_001755176.2:n.1606A>G
XR_002958670.1:n.1391A>G
XR_937825.3:n.1279+687A>G
NM_000026.4:c.1364A>G MANE Select	NP_000017.1:p.Gln455Arg
NM_001363840.2:c.1364A>G	NP_001350769.1:p.Gln455Arg
NM_001123378.3:c.1191+687A>G	NP_001116850.1:n.1191+687A>G
NM_001317923.2:c.1172A>G	NP_001304852.1:p.Gln391Arg
NM_001363840.3:c.1364A>G	NP_001350769.1:p.Gln455Arg
NR_134256.2:n.1454A>G