Canonical Allele Identifier: CA1713948898
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66087207C= , CM000669.2:g.66087207C= GRCh38
NC_000007.13:g.65552194C= , CM000669.1:g.65552194C= GRCh37
NC_000007.12:g.65189629C= NCBI36
NG_009288.1:g.16419C=

Transcript Alleles

HGVS Amino-acid change
ENST00000304874.14:c.603-127C= MANE Select ENSP00000307188.9:n.603-127C=
ENST00000362000.10:c.408-127C= ENSP00000354710.6:n.408-127C=
ENST00000380839.9:c.525-127C= ENSP00000370219.4:n.525-127C=
ENST00000395331.4:c.603-127C= ENSP00000378740.3:n.603-127C=
ENST00000395332.8:c.603-127C= ENSP00000378741.3:n.603-127C=
ENST00000671817.1:c.525-127C= ENSP00000500462.1:n.525-127C=
ENST00000672498.1:c.447-522C= ENSP00000500227.1:n.447-522C=
ENST00000672586.1:n.893C=
ENST00000672676.1:n.1158C=
ENST00000673149.1:n.415-127C=
ENST00000673350.1:n.1236C=
ENST00000673518.1:c.525-127C= ENSP00000499889.1:n.525-127C=
ENST00000673594.1:n.452-127C=
ENST00000304874.13:c.603-127C= ENSP00000307188.9:n.603-127C=
ENST00000362000.9:c.408-127C= ENSP00000354710.5:n.408-127C=
ENST00000380839.8:c.525-127C= ENSP00000370219.4:n.525-127C=
ENST00000395331.3:c.603-127C= ENSP00000378740.3:n.603-127C=
ENST00000395332.7:c.603-127C= ENSP00000378741.3:n.603-127C=
NM_000048.3:c.603-127C= NP_000039.2:n.603-127C=
NM_001024943.1:c.603-127C= NP_001020114.1:n.603-127C=
NM_001024944.1:c.603-127C= NP_001020115.1:n.603-127C=
NM_001024946.1:c.525-127C= NP_001020117.1:n.525-127C=
NM_000048.4:c.603-127C= MANE Select NP_000039.2:n.603-127C=
NM_001024943.2:c.603-127C= NP_001020114.1:n.603-127C=
NM_001024944.2:c.603-127C= NP_001020115.1:n.603-127C=
NM_001024946.2:c.525-127C= NP_001020117.1:n.525-127C=