Canonical Allele Identifier: CA1713922790

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66088877C= , CM000669.2:g.66088877C=	GRCh38
NC_000007.13:g.65553864C= , CM000669.1:g.65553864C=	GRCh37
NC_000007.12:g.65191299C=	NCBI36
NG_009288.1:g.18089C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.789C= MANE Select	ENSP00000307188.9:p.Tyr263=
ENST00000362000.10:c.594C=	ENSP00000354710.6:p.Tyr198=
ENST00000380839.9:c.711C=	ENSP00000370219.4:p.Tyr237=
ENST00000395331.4:c.789C=	ENSP00000378740.3:p.Tyr263=
ENST00000395332.8:c.789C=	ENSP00000378741.3:p.Tyr263=
ENST00000671817.1:c.711C=	ENSP00000500462.1:p.Tyr237=
ENST00000672498.1:c.*88C=	ENSP00000500227.1:n.*88C=
ENST00000672586.1:n.1548C=
ENST00000672676.1:n.1813C=
ENST00000673149.1:n.601C=
ENST00000673350.1:n.2906C=
ENST00000673518.1:c.711C=	ENSP00000499889.1:p.Tyr237=
ENST00000304874.13:c.789C=	ENSP00000307188.9:p.Tyr263=
ENST00000362000.9:c.594C=	ENSP00000354710.5:p.Tyr198=
ENST00000380839.8:c.711C=	ENSP00000370219.4:p.Tyr237=
ENST00000395331.3:c.789C=	ENSP00000378740.3:p.Tyr263=
ENST00000395332.7:c.789C=	ENSP00000378741.3:p.Tyr263=
ENST00000450043.2:c.102C=	ENSP00000396527.2:p.Tyr34=
ENST00000493708.5:n.170C=
NM_000048.3:c.789C=	NP_000039.2:p.Tyr263=
NM_001024943.1:c.789C=	NP_001020114.1:p.Tyr263=
NM_001024944.1:c.789C=	NP_001020115.1:p.Tyr263=
NM_001024946.1:c.711C=	NP_001020117.1:p.Tyr237=
NM_000048.4:c.789C= MANE Select	NP_000039.2:p.Tyr263=
NM_001024943.2:c.789C=	NP_001020114.1:p.Tyr263=
NM_001024944.2:c.789C=	NP_001020115.1:p.Tyr263=
NM_001024946.2:c.711C=	NP_001020117.1:p.Tyr237=