Canonical Allele Identifier: CA514615581

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40760907G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40364903G>A , CM000684.2:g.40364903G>A	GRCh38
NC_000022.10:g.40760907G>A , CM000684.1:g.40760907G>A	GRCh37
NC_000022.9:g.39090853G>A	NCBI36
NG_007993.1:g.23404G>A
NG_007993.2:g.23404G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*609G>A	ENSP00000485462.2:n.*609G>A
ENST00000623287.4:c.*640G>A	ENSP00000485437.1:n.*640G>A
ENST00000623632.4:c.906G>A	ENSP00000485288.2:p.Val302=
ENST00000625194.4:c.1257G>A	ENSP00000485289.2:p.Val419=
ENST00000636433.1:n.1237G>A
ENST00000636714.1:c.1215G>A	ENSP00000490946.1:p.Val405=
ENST00000637666.2:c.1191+538G>A	ENSP00000489696.2:n.1191+538G>A
ENST00000637669.1:c.1215G>A	ENSP00000489728.1:p.Val405=
ENST00000639722.1:c.*911G>A	ENSP00000492828.1:n.*911G>A
ENST00000674592.1:n.2729G>A
ENST00000675622.1:n.4282G>A
ENST00000679609.1:c.*825G>A	ENSP00000506592.1:n.*825G>A
ENST00000679656.1:n.1900G>A
ENST00000679723.1:c.1170G>A	ENSP00000505155.1:p.Val390=
ENST00000679845.1:n.1523G>A
ENST00000679904.1:n.1611G>A
ENST00000680378.1:c.1302G>A	ENSP00000505556.1:p.Val434=
ENST00000680444.1:c.*578G>A	ENSP00000505298.1:n.*578G>A
ENST00000680978.1:c.1215G>A	ENSP00000505244.1:p.Val405=
ENST00000681003.1:n.678G>A
ENST00000681159.1:n.2619G>A
ENST00000216194.11:c.1257G>A	ENSP00000216194.8:p.Val419=
ENST00000342312.9:c.1191+538G>A	ENSP00000341429.6:n.1191+538G>A
ENST00000623063.3:c.1215G>A MANE Select	ENSP00000485525.1:p.Val405=
ENST00000623387.1:n.346G>A
ENST00000625194.3:c.844G>A
NM_000026.2:c.1215G>A	NP_000017.1:p.Val405=
NM_001123378.1:c.1191+538G>A	NP_001116850.1:n.1191+538G>A
XM_011529976.1:c.1215G>A	XP_011528278.1:p.Val405=
XM_011529977.1:c.1215G>A	XP_011528279.1:p.Val405=
XM_011529978.1:c.1191+538G>A	XP_011528280.1:n.1191+538G>A
XM_011529979.1:c.1215G>A	XP_011528281.1:p.Val405=
XM_011529980.1:c.1191+538G>A	XP_011528282.1:n.1191+538G>A
XM_011529981.1:c.750G>A	XP_011528283.1:p.Val250=
XM_011529982.1:c.384G>A	XP_011528284.1:p.Val128=
XR_937824.1:n.1305G>A
XR_937825.1:n.1281+538G>A
NM_000026.3:c.1215G>A	NP_000017.1:p.Val405=
NM_001123378.2:c.1191+538G>A	NP_001116850.1:n.1191+538G>A
NM_001317923.1:c.1023G>A	NP_001304852.1:p.Val341=
NM_001363840.1:c.1215G>A	NP_001350769.1:p.Val405=
NR_134256.1:n.1305G>A
XM_011529977.3:c.1215G>A	XP_011528279.1:p.Val405=
XM_011529980.3:c.1191+538G>A	XP_011528282.1:n.1191+538G>A
XM_017028636.1:c.1170G>A	XP_016884125.1:p.Val390=
XM_017028637.1:c.1170G>A	XP_016884126.1:p.Val390=
XM_017028638.1:c.750G>A	XP_016884127.1:p.Val250=
XM_017028639.2:c.750G>A	XP_016884128.1:p.Val250=
XM_017028640.1:c.384G>A	XP_016884129.1:p.Val128=
XM_024452166.1:c.1146+538G>A	XP_024307934.1:n.1146+538G>A
XR_001755176.2:n.1457G>A
XR_002958670.1:n.1242G>A
XR_937825.3:n.1279+538G>A
NM_000026.4:c.1215G>A MANE Select	NP_000017.1:p.Val405=
NM_001363840.2:c.1215G>A	NP_001350769.1:p.Val405=
NM_001123378.3:c.1191+538G>A	NP_001116850.1:n.1191+538G>A
NM_001317923.2:c.1023G>A	NP_001304852.1:p.Val341=
NM_001363840.3:c.1215G>A	NP_001350769.1:p.Val405=
NR_134256.2:n.1305G>A