Canonical Allele Identifier: CA514615636

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40760994T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40364990T>C , CM000684.2:g.40364990T>C	GRCh38
NC_000022.10:g.40760994T>C , CM000684.1:g.40760994T>C	GRCh37
NC_000022.9:g.39090940T>C	NCBI36
NG_007993.1:g.23491T>C
NG_007993.2:g.23491T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*696T>C	ENSP00000485462.2:n.*696T>C
ENST00000623287.4:c.*727T>C	ENSP00000485437.1:n.*727T>C
ENST00000623632.4:c.993T>C	ENSP00000485288.2:p.Ser331=
ENST00000625194.4:c.1344T>C	ENSP00000485289.2:p.Ser448=
ENST00000636433.1:n.1324T>C
ENST00000636714.1:c.1302T>C	ENSP00000490946.1:p.Ser434=
ENST00000637666.2:c.1191+625T>C	ENSP00000489696.2:n.1191+625T>C
ENST00000637669.1:c.1302T>C	ENSP00000489728.1:p.Ser434=
ENST00000639722.1:c.*998T>C	ENSP00000492828.1:n.*998T>C
ENST00000674592.1:n.2816T>C
ENST00000675622.1:n.4369T>C
ENST00000679609.1:c.*912T>C	ENSP00000506592.1:n.*912T>C
ENST00000679656.1:n.1987T>C
ENST00000679723.1:c.1257T>C	ENSP00000505155.1:p.Ser419=
ENST00000679845.1:n.1610T>C
ENST00000679904.1:n.1698T>C
ENST00000680378.1:c.1389T>C	ENSP00000505556.1:p.Ser463=
ENST00000680444.1:c.*665T>C	ENSP00000505298.1:n.*665T>C
ENST00000680978.1:c.1302T>C	ENSP00000505244.1:p.Ser434=
ENST00000681003.1:n.765T>C
ENST00000681159.1:n.2706T>C
ENST00000216194.11:c.1344T>C	ENSP00000216194.8:p.Ser448=
ENST00000342312.9:c.1191+625T>C	ENSP00000341429.6:n.1191+625T>C
ENST00000423176.6:c.29T>C
ENST00000623063.3:c.1302T>C MANE Select	ENSP00000485525.1:p.Ser434=
ENST00000623387.1:n.433T>C
ENST00000623869.3:c.33T>C	ENSP00000485211.1:p.Ser11=
ENST00000624027.1:c.29T>C
ENST00000625194.3:c.931T>C
NM_000026.2:c.1302T>C	NP_000017.1:p.Ser434=
NM_001123378.1:c.1191+625T>C	NP_001116850.1:n.1191+625T>C
XM_011529976.1:c.1302T>C	XP_011528278.1:p.Ser434=
XM_011529977.1:c.1302T>C	XP_011528279.1:p.Ser434=
XM_011529978.1:c.1191+625T>C	XP_011528280.1:n.1191+625T>C
XM_011529979.1:c.1302T>C	XP_011528281.1:p.Ser434=
XM_011529980.1:c.1191+625T>C	XP_011528282.1:n.1191+625T>C
XM_011529981.1:c.837T>C	XP_011528283.1:p.Ser279=
XM_011529982.1:c.471T>C	XP_011528284.1:p.Ser157=
XR_937824.1:n.1392T>C
XR_937825.1:n.1281+625T>C
NM_000026.3:c.1302T>C	NP_000017.1:p.Ser434=
NM_001123378.2:c.1191+625T>C	NP_001116850.1:n.1191+625T>C
NM_001317923.1:c.1110T>C	NP_001304852.1:p.Ser370=
NM_001363840.1:c.1302T>C	NP_001350769.1:p.Ser434=
NR_134256.1:n.1392T>C
XM_011529977.3:c.1302T>C	XP_011528279.1:p.Ser434=
XM_011529980.3:c.1191+625T>C	XP_011528282.1:n.1191+625T>C
XM_017028636.1:c.1257T>C	XP_016884125.1:p.Ser419=
XM_017028637.1:c.1257T>C	XP_016884126.1:p.Ser419=
XM_017028638.1:c.837T>C	XP_016884127.1:p.Ser279=
XM_017028639.2:c.837T>C	XP_016884128.1:p.Ser279=
XM_017028640.1:c.471T>C	XP_016884129.1:p.Ser157=
XM_024452166.1:c.1146+625T>C	XP_024307934.1:n.1146+625T>C
XR_001755176.2:n.1544T>C
XR_002958670.1:n.1329T>C
XR_937825.3:n.1279+625T>C
NM_000026.4:c.1302T>C MANE Select	NP_000017.1:p.Ser434=
NM_001363840.2:c.1302T>C	NP_001350769.1:p.Ser434=
NM_001123378.3:c.1191+625T>C	NP_001116850.1:n.1191+625T>C
NM_001317923.2:c.1110T>C	NP_001304852.1:p.Ser370=
NM_001363840.3:c.1302T>C	NP_001350769.1:p.Ser434=
NR_134256.2:n.1392T>C