Canonical Allele Identifier: CA1713921303

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087869A= , CM000669.2:g.66087869A=	GRCh38
NC_000007.13:g.65552856A= , CM000669.1:g.65552856A=	GRCh37
NC_000007.12:g.65190291A=	NCBI36
NG_009288.1:g.17081A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.718+78A= MANE Select	ENSP00000307188.9:n.718+78A=
ENST00000362000.10:c.523+78A=	ENSP00000354710.6:n.523+78A=
ENST00000380839.9:c.640+78A=	ENSP00000370219.4:n.640+78A=
ENST00000395331.4:c.718+78A=	ENSP00000378740.3:n.718+78A=
ENST00000395332.8:c.718+78A=	ENSP00000378741.3:n.718+78A=
ENST00000671817.1:c.640+78A=	ENSP00000500462.1:n.640+78A=
ENST00000672498.1:c.*17+78A=	ENSP00000500227.1:n.*17+78A=
ENST00000672586.1:n.1477+78A=
ENST00000672676.1:n.1742+78A=
ENST00000673149.1:n.530+78A=
ENST00000673350.1:n.1898A=
ENST00000673518.1:c.640+78A=	ENSP00000499889.1:n.640+78A=
ENST00000304874.13:c.718+78A=	ENSP00000307188.9:n.718+78A=
ENST00000362000.9:c.523+78A=	ENSP00000354710.5:n.523+78A=
ENST00000380839.8:c.640+78A=	ENSP00000370219.4:n.640+78A=
ENST00000395331.3:c.718+78A=	ENSP00000378740.3:n.718+78A=
ENST00000395332.7:c.718+78A=	ENSP00000378741.3:n.718+78A=
ENST00000450043.2:c.31+78A=	ENSP00000396527.2:n.31+78A=
ENST00000493708.5:n.99+78A=
NM_000048.3:c.718+78A=	NP_000039.2:n.718+78A=
NM_001024943.1:c.718+78A=	NP_001020114.1:n.718+78A=
NM_001024944.1:c.718+78A=	NP_001020115.1:n.718+78A=
NM_001024946.1:c.640+78A=	NP_001020117.1:n.640+78A=
NM_000048.4:c.718+78A= MANE Select	NP_000039.2:n.718+78A=
NM_001024943.2:c.718+78A=	NP_001020114.1:n.718+78A=
NM_001024944.2:c.718+78A=	NP_001020115.1:n.718+78A=
NM_001024946.2:c.640+78A=	NP_001020117.1:n.640+78A=