Canonical Allele Identifier: CA1713939700

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66082417A= , CM000669.2:g.66082417A=	GRCh38
NC_000007.13:g.65547404A= , CM000669.1:g.65547404A=	GRCh37
NC_000007.12:g.65184839A=	NCBI36
NG_009288.1:g.11629A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.257A= MANE Select	ENSP00000307188.9:p.Glu86=
ENST00000362000.10:c.62A=	ENSP00000354710.6:p.Glu21=
ENST00000380839.9:c.257A=	ENSP00000370219.4:p.Glu86=
ENST00000395331.4:c.257A=	ENSP00000378740.3:p.Glu86=
ENST00000395332.8:c.257A=	ENSP00000378741.3:p.Glu86=
ENST00000671817.1:c.257A=	ENSP00000500462.1:p.Glu86=
ENST00000672498.1:c.257A=	ENSP00000500227.1:p.Glu86=
ENST00000672586.1:n.162A=
ENST00000672676.1:n.427A=
ENST00000673350.1:n.505A=
ENST00000673518.1:c.257A=	ENSP00000499889.1:p.Glu86=
ENST00000673594.1:n.106A=
ENST00000304874.13:c.257A=	ENSP00000307188.9:p.Glu86=
ENST00000362000.9:c.62A=	ENSP00000354710.5:p.Glu21=
ENST00000380839.8:c.257A=	ENSP00000370219.4:p.Glu86=
ENST00000395331.3:c.257A=	ENSP00000378740.3:p.Glu86=
ENST00000395332.7:c.257A=	ENSP00000378741.3:p.Glu86=
ENST00000487982.5:n.323A=
ENST00000496336.1:n.498A=
NM_000048.3:c.257A=	NP_000039.2:p.Glu86=
NM_001024943.1:c.257A=	NP_001020114.1:p.Glu86=
NM_001024944.1:c.257A=	NP_001020115.1:p.Glu86=
NM_001024946.1:c.257A=	NP_001020117.1:p.Glu86=
NM_000048.4:c.257A= MANE Select	NP_000039.2:p.Glu86=
NM_001024943.2:c.257A=	NP_001020114.1:p.Glu86=
NM_001024944.2:c.257A=	NP_001020115.1:p.Glu86=
NM_001024946.2:c.257A=	NP_001020117.1:p.Glu86=