Canonical Allele Identifier: CA1713947805
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66086592G= , CM000669.2:g.66086592G= GRCh38
NC_000007.13:g.65551579G= , CM000669.1:g.65551579G= GRCh37
NC_000007.12:g.65189014G= NCBI36
NG_009288.1:g.15804G=

Transcript Alleles

HGVS Amino-acid change
ENST00000304874.14:c.454G= MANE Select ENSP00000307188.9:p.Asp152=
ENST00000362000.10:c.259G= ENSP00000354710.6:p.Asp87=
ENST00000380839.9:c.454G= ENSP00000370219.4:p.Asp152=
ENST00000395331.4:c.454G= ENSP00000378740.3:p.Asp152=
ENST00000395332.8:c.454G= ENSP00000378741.3:p.Asp152=
ENST00000671817.1:c.454G= ENSP00000500462.1:p.Asp152=
ENST00000672498.1:c.447-1137G= ENSP00000500227.1:n.447-1137G=
ENST00000672586.1:n.359G=
ENST00000672676.1:n.624G=
ENST00000673149.1:n.266G=
ENST00000673350.1:n.702G=
ENST00000673518.1:c.454G= ENSP00000499889.1:p.Asp152=
ENST00000673594.1:n.303G=
ENST00000304874.13:c.454G= ENSP00000307188.9:p.Asp152=
ENST00000362000.9:c.259G= ENSP00000354710.5:p.Asp87=
ENST00000380839.8:c.454G= ENSP00000370219.4:p.Asp152=
ENST00000395331.3:c.454G= ENSP00000378740.3:p.Asp152=
ENST00000395332.7:c.454G= ENSP00000378741.3:p.Asp152=
ENST00000487982.5:n.520G=
NM_000048.3:c.454G= NP_000039.2:p.Asp152=
NM_001024943.1:c.454G= NP_001020114.1:p.Asp152=
NM_001024944.1:c.454G= NP_001020115.1:p.Asp152=
NM_001024946.1:c.454G= NP_001020117.1:p.Asp152=
NM_000048.4:c.454G= MANE Select NP_000039.2:p.Asp152=
NM_001024943.2:c.454G= NP_001020114.1:p.Asp152=
NM_001024944.2:c.454G= NP_001020115.1:p.Asp152=
NM_001024946.2:c.454G= NP_001020117.1:p.Asp152=