Canonical Allele Identifier: CA1713923272
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66089127C= , CM000669.2:g.66089127C= GRCh38
NC_000007.13:g.65554114C= , CM000669.1:g.65554114C= GRCh37
NC_000007.12:g.65191549C= NCBI36
NG_009288.1:g.18339C=

Transcript Alleles

HGVS Amino-acid change
ENST00000304874.14:c.870C= MANE Select ENSP00000307188.9:p.Pro290=
ENST00000362000.10:c.675C= ENSP00000354710.6:p.Pro225=
ENST00000380839.9:c.792C= ENSP00000370219.4:p.Pro264=
ENST00000395331.4:c.870C= ENSP00000378740.3:p.Pro290=
ENST00000395332.8:c.870C= ENSP00000378741.3:p.Pro290=
ENST00000488343.2:c.39C= ENSP00000500864.1:p.Pro13=
ENST00000671817.1:c.792C= ENSP00000500462.1:p.Pro264=
ENST00000672498.1:c.*169C= ENSP00000500227.1:n.*169C=
ENST00000672586.1:n.1629C=
ENST00000672676.1:n.1894C=
ENST00000673149.1:n.682C=
ENST00000673350.1:n.2987C=
ENST00000673518.1:c.792C= ENSP00000499889.1:p.Pro264=
ENST00000304874.13:c.870C= ENSP00000307188.9:p.Pro290=
ENST00000362000.9:c.675C= ENSP00000354710.5:p.Pro225=
ENST00000380839.8:c.792C= ENSP00000370219.4:p.Pro264=
ENST00000395331.3:c.870C= ENSP00000378740.3:p.Pro290=
ENST00000395332.7:c.870C= ENSP00000378741.3:p.Pro290=
ENST00000450043.2:c.183C= ENSP00000396527.2:p.Pro61=
ENST00000488343.1:n.39C=
ENST00000493708.5:n.251C=
NM_000048.3:c.870C= NP_000039.2:p.Pro290=
NM_001024943.1:c.870C= NP_001020114.1:p.Pro290=
NM_001024944.1:c.870C= NP_001020115.1:p.Pro290=
NM_001024946.1:c.792C= NP_001020117.1:p.Pro264=
NM_000048.4:c.870C= MANE Select NP_000039.2:p.Pro290=
NM_001024943.2:c.870C= NP_001020114.1:p.Pro290=
NM_001024944.2:c.870C= NP_001020115.1:p.Pro290=
NM_001024946.2:c.792C= NP_001020117.1:p.Pro264=