Canonical Allele Identifier: CA1713923261

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089122A= , CM000669.2:g.66089122A=	GRCh38
NC_000007.13:g.65554109A= , CM000669.1:g.65554109A=	GRCh37
NC_000007.12:g.65191544A=	NCBI36
NG_009288.1:g.18334A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.865A= MANE Select	ENSP00000307188.9:p.Asn289=
ENST00000362000.10:c.670A=	ENSP00000354710.6:p.Asn224=
ENST00000380839.9:c.787A=	ENSP00000370219.4:p.Asn263=
ENST00000395331.4:c.865A=	ENSP00000378740.3:p.Asn289=
ENST00000395332.8:c.865A=	ENSP00000378741.3:p.Asn289=
ENST00000488343.2:c.34A=	ENSP00000500864.1:p.Asn12=
ENST00000671817.1:c.787A=	ENSP00000500462.1:p.Asn263=
ENST00000672498.1:c.*164A=	ENSP00000500227.1:n.*164A=
ENST00000672586.1:n.1624A=
ENST00000672676.1:n.1889A=
ENST00000673149.1:n.677A=
ENST00000673350.1:n.2982A=
ENST00000673518.1:c.787A=	ENSP00000499889.1:p.Asn263=
ENST00000304874.13:c.865A=	ENSP00000307188.9:p.Asn289=
ENST00000362000.9:c.670A=	ENSP00000354710.5:p.Asn224=
ENST00000380839.8:c.787A=	ENSP00000370219.4:p.Asn263=
ENST00000395331.3:c.865A=	ENSP00000378740.3:p.Asn289=
ENST00000395332.7:c.865A=	ENSP00000378741.3:p.Asn289=
ENST00000450043.2:c.178A=	ENSP00000396527.2:p.Asn60=
ENST00000488343.1:n.34A=
ENST00000493708.5:n.246A=
NM_000048.3:c.865A=	NP_000039.2:p.Asn289=
NM_001024943.1:c.865A=	NP_001020114.1:p.Asn289=
NM_001024944.1:c.865A=	NP_001020115.1:p.Asn289=
NM_001024946.1:c.787A=	NP_001020117.1:p.Asn263=
NM_000048.4:c.865A= MANE Select	NP_000039.2:p.Asn289=
NM_001024943.2:c.865A=	NP_001020114.1:p.Asn289=
NM_001024944.2:c.865A=	NP_001020115.1:p.Asn289=
NM_001024946.2:c.787A=	NP_001020117.1:p.Asn263=