Canonical Allele Identifier: CA1713923116
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66089070C= , CM000669.2:g.66089070C= GRCh38
NC_000007.13:g.65554057C= , CM000669.1:g.65554057C= GRCh37
NC_000007.12:g.65191492C= NCBI36
NG_009288.1:g.18282C=

Transcript Alleles

HGVS Amino-acid change
ENST00000304874.14:c.834-21C= MANE Select ENSP00000307188.9:n.834-21C=
ENST00000362000.10:c.639-21C= ENSP00000354710.6:n.639-21C=
ENST00000380839.9:c.756-21C= ENSP00000370219.4:n.756-21C=
ENST00000395331.4:c.834-21C= ENSP00000378740.3:n.834-21C=
ENST00000395332.8:c.834-21C= ENSP00000378741.3:n.834-21C=
ENST00000488343.2:c.3-21C= ENSP00000500864.1:n.3-21C=
ENST00000671817.1:c.756-21C= ENSP00000500462.1:n.756-21C=
ENST00000672498.1:c.*133-21C= ENSP00000500227.1:n.*133-21C=
ENST00000672586.1:n.1593-21C=
ENST00000672676.1:n.1858-21C=
ENST00000673149.1:n.646-21C=
ENST00000673350.1:n.2951-21C=
ENST00000673518.1:c.756-21C= ENSP00000499889.1:n.756-21C=
ENST00000304874.13:c.834-21C= ENSP00000307188.9:n.834-21C=
ENST00000362000.9:c.639-21C= ENSP00000354710.5:n.639-21C=
ENST00000380839.8:c.756-21C= ENSP00000370219.4:n.756-21C=
ENST00000395331.3:c.834-21C= ENSP00000378740.3:n.834-21C=
ENST00000395332.7:c.834-21C= ENSP00000378741.3:n.834-21C=
ENST00000450043.2:c.147-21C= ENSP00000396527.2:n.147-21C=
ENST00000493708.5:n.215-21C=
NM_000048.3:c.834-21C= NP_000039.2:n.834-21C=
NM_001024943.1:c.834-21C= NP_001020114.1:n.834-21C=
NM_001024944.1:c.834-21C= NP_001020115.1:n.834-21C=
NM_001024946.1:c.756-21C= NP_001020117.1:n.756-21C=
NM_000048.4:c.834-21C= MANE Select NP_000039.2:n.834-21C=
NM_001024943.2:c.834-21C= NP_001020114.1:n.834-21C=
NM_001024944.2:c.834-21C= NP_001020115.1:n.834-21C=
NM_001024946.2:c.756-21C= NP_001020117.1:n.756-21C=