Canonical Allele Identifier: CA1713923206

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089103C= , CM000669.2:g.66089103C=	GRCh38
NC_000007.13:g.65554090C= , CM000669.1:g.65554090C=	GRCh37
NC_000007.12:g.65191525C=	NCBI36
NG_009288.1:g.18315C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.846C= MANE Select	ENSP00000307188.9:p.Ser282=
ENST00000362000.10:c.651C=	ENSP00000354710.6:p.Ser217=
ENST00000380839.9:c.768C=	ENSP00000370219.4:p.Ser256=
ENST00000395331.4:c.846C=	ENSP00000378740.3:p.Ser282=
ENST00000395332.8:c.846C=	ENSP00000378741.3:p.Ser282=
ENST00000488343.2:c.15C=	ENSP00000500864.1:p.Ser5=
ENST00000671817.1:c.768C=	ENSP00000500462.1:p.Ser256=
ENST00000672498.1:c.*145C=	ENSP00000500227.1:n.*145C=
ENST00000672586.1:n.1605C=
ENST00000672676.1:n.1870C=
ENST00000673149.1:n.658C=
ENST00000673350.1:n.2963C=
ENST00000673518.1:c.768C=	ENSP00000499889.1:p.Ser256=
ENST00000304874.13:c.846C=	ENSP00000307188.9:p.Ser282=
ENST00000362000.9:c.651C=	ENSP00000354710.5:p.Ser217=
ENST00000380839.8:c.768C=	ENSP00000370219.4:p.Ser256=
ENST00000395331.3:c.846C=	ENSP00000378740.3:p.Ser282=
ENST00000395332.7:c.846C=	ENSP00000378741.3:p.Ser282=
ENST00000450043.2:c.159C=	ENSP00000396527.2:p.Ser53=
ENST00000488343.1:n.15C=
ENST00000493708.5:n.227C=
NM_000048.3:c.846C=	NP_000039.2:p.Ser282=
NM_001024943.1:c.846C=	NP_001020114.1:p.Ser282=
NM_001024944.1:c.846C=	NP_001020115.1:p.Ser282=
NM_001024946.1:c.768C=	NP_001020117.1:p.Ser256=
NM_000048.4:c.846C= MANE Select	NP_000039.2:p.Ser282=
NM_001024943.2:c.846C=	NP_001020114.1:p.Ser282=
NM_001024944.2:c.846C=	NP_001020115.1:p.Ser282=
NM_001024946.2:c.768C=	NP_001020117.1:p.Ser256=