Canonical Allele Identifier: CA1713947980

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66086645G= , CM000669.2:g.66086645G=	GRCh38
NC_000007.13:g.65551632G= , CM000669.1:g.65551632G=	GRCh37
NC_000007.12:g.65189067G=	NCBI36
NG_009288.1:g.15857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.507G= MANE Select	ENSP00000307188.9:p.Trp169=
ENST00000362000.10:c.312G=	ENSP00000354710.6:p.Trp104=
ENST00000380839.9:c.507G=	ENSP00000370219.4:p.Trp169=
ENST00000395331.4:c.507G=	ENSP00000378740.3:p.Trp169=
ENST00000395332.8:c.507G=	ENSP00000378741.3:p.Trp169=
ENST00000671817.1:c.507G=	ENSP00000500462.1:p.Trp169=
ENST00000672498.1:c.447-1084G=	ENSP00000500227.1:n.447-1084G=
ENST00000672586.1:n.412G=
ENST00000672676.1:n.677G=
ENST00000673149.1:n.319G=
ENST00000673350.1:n.755G=
ENST00000673518.1:c.507G=	ENSP00000499889.1:p.Trp169=
ENST00000673594.1:n.356G=
ENST00000304874.13:c.507G=	ENSP00000307188.9:p.Trp169=
ENST00000362000.9:c.312G=	ENSP00000354710.5:p.Trp104=
ENST00000380839.8:c.507G=	ENSP00000370219.4:p.Trp169=
ENST00000395331.3:c.507G=	ENSP00000378740.3:p.Trp169=
ENST00000395332.7:c.507G=	ENSP00000378741.3:p.Trp169=
ENST00000487982.5:n.573G=
NM_000048.3:c.507G=	NP_000039.2:p.Trp169=
NM_001024943.1:c.507G=	NP_001020114.1:p.Trp169=
NM_001024944.1:c.507G=	NP_001020115.1:p.Trp169=
NM_001024946.1:c.507G=	NP_001020117.1:p.Trp169=
NM_000048.4:c.507G= MANE Select	NP_000039.2:p.Trp169=
NM_001024943.2:c.507G=	NP_001020114.1:p.Trp169=
NM_001024944.2:c.507G=	NP_001020115.1:p.Trp169=
NM_001024946.2:c.507G=	NP_001020117.1:p.Trp169=