Canonical Allele Identifier: CA514615653

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40761024G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40365020G>A , CM000684.2:g.40365020G>A	GRCh38
NC_000022.10:g.40761024G>A , CM000684.1:g.40761024G>A	GRCh37
NC_000022.9:g.39090970G>A	NCBI36
NG_007993.1:g.23521G>A
NG_007993.2:g.23521G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*726G>A	ENSP00000485462.2:n.*726G>A
ENST00000623287.4:c.*757G>A	ENSP00000485437.1:n.*757G>A
ENST00000623632.4:c.1023G>A	ENSP00000485288.2:p.Leu341=
ENST00000625194.4:c.1374G>A	ENSP00000485289.2:p.Leu458=
ENST00000636433.1:n.1354G>A
ENST00000636714.1:c.1332G>A	ENSP00000490946.1:p.Leu444=
ENST00000637666.2:c.1191+655G>A	ENSP00000489696.2:n.1191+655G>A
ENST00000637669.1:c.1332G>A	ENSP00000489728.1:p.Leu444=
ENST00000639722.1:c.*1028G>A	ENSP00000492828.1:n.*1028G>A
ENST00000674592.1:n.2846G>A
ENST00000675622.1:n.4399G>A
ENST00000679609.1:c.*942G>A	ENSP00000506592.1:n.*942G>A
ENST00000679656.1:n.2017G>A
ENST00000679723.1:c.1287G>A	ENSP00000505155.1:p.Leu429=
ENST00000679845.1:n.1640G>A
ENST00000679904.1:n.1728G>A
ENST00000680378.1:c.1419G>A	ENSP00000505556.1:p.Leu473=
ENST00000680444.1:c.*695G>A	ENSP00000505298.1:n.*695G>A
ENST00000680978.1:c.1332G>A	ENSP00000505244.1:p.Leu444=
ENST00000681003.1:n.795G>A
ENST00000681159.1:n.2736G>A
ENST00000216194.11:c.1374G>A	ENSP00000216194.8:p.Leu458=
ENST00000342312.9:c.1191+655G>A	ENSP00000341429.6:n.1191+655G>A
ENST00000423176.6:c.59G>A
ENST00000623063.3:c.1332G>A MANE Select	ENSP00000485525.1:p.Leu444=
ENST00000623387.1:n.463G>A
ENST00000623869.3:c.63G>A	ENSP00000485211.1:p.Leu21=
ENST00000624027.1:c.59G>A
ENST00000625194.3:c.961G>A
NM_000026.2:c.1332G>A	NP_000017.1:p.Leu444=
NM_001123378.1:c.1191+655G>A	NP_001116850.1:n.1191+655G>A
XM_011529976.1:c.1332G>A	XP_011528278.1:p.Leu444=
XM_011529977.1:c.1332G>A	XP_011528279.1:p.Leu444=
XM_011529978.1:c.1191+655G>A	XP_011528280.1:n.1191+655G>A
XM_011529979.1:c.1332G>A	XP_011528281.1:p.Leu444=
XM_011529980.1:c.1191+655G>A	XP_011528282.1:n.1191+655G>A
XM_011529981.1:c.867G>A	XP_011528283.1:p.Leu289=
XM_011529982.1:c.501G>A	XP_011528284.1:p.Leu167=
XR_937824.1:n.1422G>A
XR_937825.1:n.1281+655G>A
NM_000026.3:c.1332G>A	NP_000017.1:p.Leu444=
NM_001123378.2:c.1191+655G>A	NP_001116850.1:n.1191+655G>A
NM_001317923.1:c.1140G>A	NP_001304852.1:p.Leu380=
NM_001363840.1:c.1332G>A	NP_001350769.1:p.Leu444=
NR_134256.1:n.1422G>A
XM_011529977.3:c.1332G>A	XP_011528279.1:p.Leu444=
XM_011529980.3:c.1191+655G>A	XP_011528282.1:n.1191+655G>A
XM_017028636.1:c.1287G>A	XP_016884125.1:p.Leu429=
XM_017028637.1:c.1287G>A	XP_016884126.1:p.Leu429=
XM_017028638.1:c.867G>A	XP_016884127.1:p.Leu289=
XM_017028639.2:c.867G>A	XP_016884128.1:p.Leu289=
XM_017028640.1:c.501G>A	XP_016884129.1:p.Leu167=
XM_024452166.1:c.1146+655G>A	XP_024307934.1:n.1146+655G>A
XR_001755176.2:n.1574G>A
XR_002958670.1:n.1359G>A
XR_937825.3:n.1279+655G>A
NM_000026.4:c.1332G>A MANE Select	NP_000017.1:p.Leu444=
NM_001363840.2:c.1332G>A	NP_001350769.1:p.Leu444=
NM_001123378.3:c.1191+655G>A	NP_001116850.1:n.1191+655G>A
NM_001317923.2:c.1140G>A	NP_001304852.1:p.Leu380=
NM_001363840.3:c.1332G>A	NP_001350769.1:p.Leu444=
NR_134256.2:n.1422G>A