Canonical Allele Identifier: CA10247964

Gene: ADSL

Linked Data

• ClinVar Variation Id: 459614
• ClinVar RCV Id: RCV000556894
• dbSNP Id: rs781253590
• ExAC: 22:40760904 A / C
• gnomAD v2: 22-40760904-A-C
• gnomAD v4: 22-40364900-A-C
• MyVariant Identifiers: chr22:g.40760904A>C (hg19) ; chr22:g.40364900A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40364900A>C , CM000684.2:g.40364900A>C	GRCh38
NC_000022.10:g.40760904A>C , CM000684.1:g.40760904A>C	GRCh37
NC_000022.9:g.39090850A>C	NCBI36
NG_007993.1:g.23401A>C
NG_007993.2:g.23401A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*606A>C	ENSP00000485462.2:n.*606A>C
ENST00000623287.4:c.*637A>C	ENSP00000485437.1:n.*637A>C
ENST00000623632.4:c.903A>C	ENSP00000485288.2:p.Arg301Ser
ENST00000625194.4:c.1254A>C	ENSP00000485289.2:p.Arg418Ser
ENST00000636433.1:n.1234A>C
ENST00000636714.1:c.1212A>C	ENSP00000490946.1:p.Arg404Ser
ENST00000637666.2:c.1191+535A>C	ENSP00000489696.2:n.1191+535A>C
ENST00000637669.1:c.1212A>C	ENSP00000489728.1:p.Arg404Ser
ENST00000639722.1:c.*908A>C	ENSP00000492828.1:n.*908A>C
ENST00000674592.1:n.2726A>C
ENST00000675622.1:n.4279A>C
ENST00000679609.1:c.*822A>C	ENSP00000506592.1:n.*822A>C
ENST00000679656.1:n.1897A>C
ENST00000679723.1:c.1167A>C	ENSP00000505155.1:p.Arg389Ser
ENST00000679845.1:n.1520A>C
ENST00000679904.1:n.1608A>C
ENST00000680378.1:c.1299A>C	ENSP00000505556.1:p.Arg433Ser
ENST00000680444.1:c.*575A>C	ENSP00000505298.1:n.*575A>C
ENST00000680978.1:c.1212A>C	ENSP00000505244.1:p.Arg404Ser
ENST00000681003.1:n.675A>C
ENST00000681159.1:n.2616A>C
ENST00000216194.11:c.1254A>C	ENSP00000216194.8:p.Arg418Ser
ENST00000342312.9:c.1191+535A>C	ENSP00000341429.6:n.1191+535A>C
ENST00000623063.3:c.1212A>C MANE Select	ENSP00000485525.1:p.Arg404Ser
ENST00000623387.1:n.343A>C
ENST00000625194.3:c.841A>C
NM_000026.2:c.1212A>C	NP_000017.1:p.Arg404Ser
NM_001123378.1:c.1191+535A>C	NP_001116850.1:n.1191+535A>C
XM_011529976.1:c.1212A>C	XP_011528278.1:p.Arg404Ser
XM_011529977.1:c.1212A>C	XP_011528279.1:p.Arg404Ser
XM_011529978.1:c.1191+535A>C	XP_011528280.1:n.1191+535A>C
XM_011529979.1:c.1212A>C	XP_011528281.1:p.Arg404Ser
XM_011529980.1:c.1191+535A>C	XP_011528282.1:n.1191+535A>C
XM_011529981.1:c.747A>C	XP_011528283.1:p.Arg249Ser
XM_011529982.1:c.381A>C	XP_011528284.1:p.Arg127Ser
XR_937824.1:n.1302A>C
XR_937825.1:n.1281+535A>C
NM_000026.3:c.1212A>C	NP_000017.1:p.Arg404Ser
NM_001123378.2:c.1191+535A>C	NP_001116850.1:n.1191+535A>C
NM_001317923.1:c.1020A>C	NP_001304852.1:p.Arg340Ser
NM_001363840.1:c.1212A>C	NP_001350769.1:p.Arg404Ser
NR_134256.1:n.1302A>C
XM_011529977.3:c.1212A>C	XP_011528279.1:p.Arg404Ser
XM_011529980.3:c.1191+535A>C	XP_011528282.1:n.1191+535A>C
XM_017028636.1:c.1167A>C	XP_016884125.1:p.Arg389Ser
XM_017028637.1:c.1167A>C	XP_016884126.1:p.Arg389Ser
XM_017028638.1:c.747A>C	XP_016884127.1:p.Arg249Ser
XM_017028639.2:c.747A>C	XP_016884128.1:p.Arg249Ser
XM_017028640.1:c.381A>C	XP_016884129.1:p.Arg127Ser
XM_024452166.1:c.1146+535A>C	XP_024307934.1:n.1146+535A>C
XR_001755176.2:n.1454A>C
XR_002958670.1:n.1239A>C
XR_937825.3:n.1279+535A>C
NM_000026.4:c.1212A>C MANE Select	NP_000017.1:p.Arg404Ser
NM_001363840.2:c.1212A>C	NP_001350769.1:p.Arg404Ser
NM_001123378.3:c.1191+535A>C	NP_001116850.1:n.1191+535A>C
NM_001317923.2:c.1020A>C	NP_001304852.1:p.Arg340Ser
NM_001363840.3:c.1212A>C	NP_001350769.1:p.Arg404Ser
NR_134256.2:n.1302A>C