Canonical Allele Identifier: CA1713948299
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66086790C= , CM000669.2:g.66086790C= GRCh38
NC_000007.13:g.65551777C= , CM000669.1:g.65551777C= GRCh37
NC_000007.12:g.65189212C= NCBI36
NG_009288.1:g.16002C=

Transcript Alleles

HGVS Amino-acid change
ENST00000304874.14:c.571C= MANE Select ENSP00000307188.9:p.Arg191=
ENST00000362000.10:c.376C= ENSP00000354710.6:p.Arg126=
ENST00000380839.9:c.524+128C= ENSP00000370219.4:n.524+128C=
ENST00000395331.4:c.571C= ENSP00000378740.3:p.Arg191=
ENST00000395332.8:c.571C= ENSP00000378741.3:p.Arg191=
ENST00000671817.1:c.524+128C= ENSP00000500462.1:n.524+128C=
ENST00000672498.1:c.447-939C= ENSP00000500227.1:n.447-939C=
ENST00000672586.1:n.476C=
ENST00000672676.1:n.741C=
ENST00000673149.1:n.383C=
ENST00000673350.1:n.819C=
ENST00000673518.1:c.524+128C= ENSP00000499889.1:n.524+128C=
ENST00000673594.1:n.420C=
ENST00000304874.13:c.571C= ENSP00000307188.9:p.Arg191=
ENST00000362000.9:c.376C= ENSP00000354710.5:p.Arg126=
ENST00000380839.8:c.524+128C= ENSP00000370219.4:n.524+128C=
ENST00000395331.3:c.571C= ENSP00000378740.3:p.Arg191=
ENST00000395332.7:c.571C= ENSP00000378741.3:p.Arg191=
ENST00000487982.5:n.637C=
NM_000048.3:c.571C= NP_000039.2:p.Arg191=
NM_001024943.1:c.571C= NP_001020114.1:p.Arg191=
NM_001024944.1:c.571C= NP_001020115.1:p.Arg191=
NM_001024946.1:c.524+128C= NP_001020117.1:n.524+128C=
NM_000048.4:c.571C= MANE Select NP_000039.2:p.Arg191=
NM_001024943.2:c.571C= NP_001020114.1:p.Arg191=
NM_001024944.2:c.571C= NP_001020115.1:p.Arg191=
NM_001024946.2:c.524+128C= NP_001020117.1:n.524+128C=