Canonical Allele Identifier: CA1713948142
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66086749C= , CM000669.2:g.66086749C= GRCh38
NC_000007.13:g.65551736C= , CM000669.1:g.65551736C= GRCh37
NC_000007.12:g.65189171C= NCBI36
NG_009288.1:g.15961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304874.14:c.530C= MANE Select ENSP00000307188.9:p.Ala177=
ENST00000362000.10:c.335C= ENSP00000354710.6:p.Ala112=
ENST00000380839.9:c.524+87C= ENSP00000370219.4:n.524+87C=
ENST00000395331.4:c.530C= ENSP00000378740.3:p.Ala177=
ENST00000395332.8:c.530C= ENSP00000378741.3:p.Ala177=
ENST00000671817.1:c.524+87C= ENSP00000500462.1:n.524+87C=
ENST00000672498.1:c.447-980C= ENSP00000500227.1:n.447-980C=
ENST00000672586.1:n.435C=
ENST00000672676.1:n.700C=
ENST00000673149.1:n.342C=
ENST00000673350.1:n.778C=
ENST00000673518.1:c.524+87C= ENSP00000499889.1:n.524+87C=
ENST00000673594.1:n.379C=
ENST00000304874.13:c.530C= ENSP00000307188.9:p.Ala177=
ENST00000362000.9:c.335C= ENSP00000354710.5:p.Ala112=
ENST00000380839.8:c.524+87C= ENSP00000370219.4:n.524+87C=
ENST00000395331.3:c.530C= ENSP00000378740.3:p.Ala177=
ENST00000395332.7:c.530C= ENSP00000378741.3:p.Ala177=
ENST00000487982.5:n.596C=
NM_000048.3:c.530C= NP_000039.2:p.Ala177=
NM_001024943.1:c.530C= NP_001020114.1:p.Ala177=
NM_001024944.1:c.530C= NP_001020115.1:p.Ala177=
NM_001024946.1:c.524+87C= NP_001020117.1:n.524+87C=
NM_000048.4:c.530C= MANE Select NP_000039.2:p.Ala177=
NM_001024943.2:c.530C= NP_001020114.1:p.Ala177=
NM_001024944.2:c.530C= NP_001020115.1:p.Ala177=
NM_001024946.2:c.524+87C= NP_001020117.1:n.524+87C=