Canonical Allele Identifier: CA1713950222

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087708T= , CM000669.2:g.66087708T=	GRCh38
NC_000007.13:g.65552695T= , CM000669.1:g.65552695T=	GRCh37
NC_000007.12:g.65190130T=	NCBI36
NG_009288.1:g.16920T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.656-21T= MANE Select	ENSP00000307188.9:n.656-21T=
ENST00000362000.10:c.461-21T=	ENSP00000354710.6:n.461-21T=
ENST00000380839.9:c.578-21T=	ENSP00000370219.4:n.578-21T=
ENST00000395331.4:c.656-21T=	ENSP00000378740.3:n.656-21T=
ENST00000395332.8:c.656-21T=	ENSP00000378741.3:n.656-21T=
ENST00000671817.1:c.578-21T=	ENSP00000500462.1:n.578-21T=
ENST00000672498.1:c.447-21T=	ENSP00000500227.1:n.447-21T=
ENST00000672586.1:n.1394T=
ENST00000672676.1:n.1659T=
ENST00000673149.1:n.468-21T=
ENST00000673350.1:n.1737T=
ENST00000673518.1:c.578-21T=	ENSP00000499889.1:n.578-21T=
ENST00000304874.13:c.656-21T=	ENSP00000307188.9:n.656-21T=
ENST00000362000.9:c.461-21T=	ENSP00000354710.5:n.461-21T=
ENST00000380839.8:c.578-21T=	ENSP00000370219.4:n.578-21T=
ENST00000395331.3:c.656-21T=	ENSP00000378740.3:n.656-21T=
ENST00000395332.7:c.656-21T=	ENSP00000378741.3:n.656-21T=
ENST00000493708.5:n.16T=
NM_000048.3:c.656-21T=	NP_000039.2:n.656-21T=
NM_001024943.1:c.656-21T=	NP_001020114.1:n.656-21T=
NM_001024944.1:c.656-21T=	NP_001020115.1:n.656-21T=
NM_001024946.1:c.578-21T=	NP_001020117.1:n.578-21T=
NM_000048.4:c.656-21T= MANE Select	NP_000039.2:n.656-21T=
NM_001024943.2:c.656-21T=	NP_001020114.1:n.656-21T=
NM_001024944.2:c.656-21T=	NP_001020115.1:n.656-21T=
NM_001024946.2:c.578-21T=	NP_001020117.1:n.578-21T=