Canonical Allele Identifier: CA411647708

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40760920G>C (hg19) ; chr22:g.40364916G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40364916G>C , CM000684.2:g.40364916G>C	GRCh38
NC_000022.10:g.40760920G>C , CM000684.1:g.40760920G>C	GRCh37
NC_000022.9:g.39090866G>C	NCBI36
NG_007993.1:g.23417G>C
NG_007993.2:g.23417G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*622G>C	ENSP00000485462.2:n.*622G>C
ENST00000623287.4:c.*653G>C	ENSP00000485437.1:n.*653G>C
ENST00000623632.4:c.919G>C	ENSP00000485288.2:p.Ala307Pro
ENST00000625194.4:c.1270G>C	ENSP00000485289.2:p.Ala424Pro
ENST00000636433.1:n.1250G>C
ENST00000636714.1:c.1228G>C	ENSP00000490946.1:p.Ala410Pro
ENST00000637666.2:c.1191+551G>C	ENSP00000489696.2:n.1191+551G>C
ENST00000637669.1:c.1228G>C	ENSP00000489728.1:p.Ala410Pro
ENST00000639722.1:c.*924G>C	ENSP00000492828.1:n.*924G>C
ENST00000674592.1:n.2742G>C
ENST00000675622.1:n.4295G>C
ENST00000679609.1:c.*838G>C	ENSP00000506592.1:n.*838G>C
ENST00000679656.1:n.1913G>C
ENST00000679723.1:c.1183G>C	ENSP00000505155.1:p.Ala395Pro
ENST00000679845.1:n.1536G>C
ENST00000679904.1:n.1624G>C
ENST00000680378.1:c.1315G>C	ENSP00000505556.1:p.Ala439Pro
ENST00000680444.1:c.*591G>C	ENSP00000505298.1:n.*591G>C
ENST00000680978.1:c.1228G>C	ENSP00000505244.1:p.Ala410Pro
ENST00000681003.1:n.691G>C
ENST00000681159.1:n.2632G>C
ENST00000216194.11:c.1270G>C	ENSP00000216194.8:p.Ala424Pro
ENST00000342312.9:c.1191+551G>C	ENSP00000341429.6:n.1191+551G>C
ENST00000623063.3:c.1228G>C MANE Select	ENSP00000485525.1:p.Ala410Pro
ENST00000623387.1:n.359G>C
ENST00000625194.3:c.857G>C
NM_000026.2:c.1228G>C	NP_000017.1:p.Ala410Pro
NM_001123378.1:c.1191+551G>C	NP_001116850.1:n.1191+551G>C
XM_011529976.1:c.1228G>C	XP_011528278.1:p.Ala410Pro
XM_011529977.1:c.1228G>C	XP_011528279.1:p.Ala410Pro
XM_011529978.1:c.1191+551G>C	XP_011528280.1:n.1191+551G>C
XM_011529979.1:c.1228G>C	XP_011528281.1:p.Ala410Pro
XM_011529980.1:c.1191+551G>C	XP_011528282.1:n.1191+551G>C
XM_011529981.1:c.763G>C	XP_011528283.1:p.Ala255Pro
XM_011529982.1:c.397G>C	XP_011528284.1:p.Ala133Pro
XR_937824.1:n.1318G>C
XR_937825.1:n.1281+551G>C
NM_000026.3:c.1228G>C	NP_000017.1:p.Ala410Pro
NM_001123378.2:c.1191+551G>C	NP_001116850.1:n.1191+551G>C
NM_001317923.1:c.1036G>C	NP_001304852.1:p.Ala346Pro
NM_001363840.1:c.1228G>C	NP_001350769.1:p.Ala410Pro
NR_134256.1:n.1318G>C
XM_011529977.3:c.1228G>C	XP_011528279.1:p.Ala410Pro
XM_011529980.3:c.1191+551G>C	XP_011528282.1:n.1191+551G>C
XM_017028636.1:c.1183G>C	XP_016884125.1:p.Ala395Pro
XM_017028637.1:c.1183G>C	XP_016884126.1:p.Ala395Pro
XM_017028638.1:c.763G>C	XP_016884127.1:p.Ala255Pro
XM_017028639.2:c.763G>C	XP_016884128.1:p.Ala255Pro
XM_017028640.1:c.397G>C	XP_016884129.1:p.Ala133Pro
XM_024452166.1:c.1146+551G>C	XP_024307934.1:n.1146+551G>C
XR_001755176.2:n.1470G>C
XR_002958670.1:n.1255G>C
XR_937825.3:n.1279+551G>C
NM_000026.4:c.1228G>C MANE Select	NP_000017.1:p.Ala410Pro
NM_001363840.2:c.1228G>C	NP_001350769.1:p.Ala410Pro
NM_001123378.3:c.1191+551G>C	NP_001116850.1:n.1191+551G>C
NM_001317923.2:c.1036G>C	NP_001304852.1:p.Ala346Pro
NM_001363840.3:c.1228G>C	NP_001350769.1:p.Ala410Pro
NR_134256.2:n.1318G>C