Canonical Allele Identifier: CA2683084803
Gene: ASL HGNC NCBI

Linked Data

gnomAD v4: 7-66088984-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66088984G>A , CM000669.2:g.66088984G>A GRCh38
NC_000007.13:g.65553971G>A , CM000669.1:g.65553971G>A GRCh37
NC_000007.12:g.65191406G>A NCBI36
NG_009288.1:g.18196G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304874.14:c.833+63G>A MANE Select ENSP00000307188.9:n.833+63G>A
ENST00000362000.10:c.638+63G>A ENSP00000354710.6:n.638+63G>A
ENST00000380839.9:c.755+63G>A ENSP00000370219.4:n.755+63G>A
ENST00000395331.4:c.833+63G>A ENSP00000378740.3:n.833+63G>A
ENST00000395332.8:c.833+63G>A ENSP00000378741.3:n.833+63G>A
ENST00000488343.2:c.2+63G>A ENSP00000500864.1:n.2+63G>A
ENST00000671817.1:c.755+63G>A ENSP00000500462.1:n.755+63G>A
ENST00000672498.1:c.*132+63G>A ENSP00000500227.1:n.*132+63G>A
ENST00000672586.1:n.1592+63G>A
ENST00000672676.1:n.1857+63G>A
ENST00000673149.1:n.645+63G>A
ENST00000673350.1:n.2950+63G>A
ENST00000673518.1:c.755+63G>A ENSP00000499889.1:n.755+63G>A
ENST00000304874.13:c.833+63G>A ENSP00000307188.9:n.833+63G>A
ENST00000362000.9:c.638+63G>A ENSP00000354710.5:n.638+63G>A
ENST00000380839.8:c.755+63G>A ENSP00000370219.4:n.755+63G>A
ENST00000395331.3:c.833+63G>A ENSP00000378740.3:n.833+63G>A
ENST00000395332.7:c.833+63G>A ENSP00000378741.3:n.833+63G>A
ENST00000450043.2:c.146+63G>A ENSP00000396527.2:n.146+63G>A
ENST00000493708.5:n.214+63G>A
NM_000048.3:c.833+63G>A NP_000039.2:n.833+63G>A
NM_001024943.1:c.833+63G>A NP_001020114.1:n.833+63G>A
NM_001024944.1:c.833+63G>A NP_001020115.1:n.833+63G>A
NM_001024946.1:c.755+63G>A NP_001020117.1:n.755+63G>A
NM_000048.4:c.833+63G>A MANE Select NP_000039.2:n.833+63G>A
NM_001024943.2:c.833+63G>A NP_001020114.1:n.833+63G>A
NM_001024944.2:c.833+63G>A NP_001020115.1:n.833+63G>A
NM_001024946.2:c.755+63G>A NP_001020117.1:n.755+63G>A