Canonical Allele Identifier: CA312343
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 203625
dbSNP Id: rs143793815
gnomAD v2: 7-65548107-C-T
gnomAD v3: 7-66083120-C-T
gnomAD v4: 7-66083120-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66083120C>T , CM000669.2:g.66083120C>T GRCh38
NC_000007.13:g.65548107C>T , CM000669.1:g.65548107C>T GRCh37
NC_000007.12:g.65185542C>T NCBI36
NG_009288.1:g.12332C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000304874.14:c.392C>T MANE Select ENSP00000307188.9:p.Thr131Met
ENST00000362000.10:c.197C>T ENSP00000354710.6:p.Thr66Met
ENST00000380839.9:c.392C>T ENSP00000370219.4:p.Thr131Met
ENST00000395331.4:c.392C>T ENSP00000378740.3:p.Thr131Met
ENST00000395332.8:c.392C>T ENSP00000378741.3:p.Thr131Met
ENST00000671817.1:c.392C>T ENSP00000500462.1:p.Thr131Met
ENST00000672498.1:c.392C>T ENSP00000500227.1:p.Thr131Met
ENST00000672586.1:n.297C>T
ENST00000672676.1:n.562C>T
ENST00000673149.1:n.204C>T
ENST00000673350.1:n.640C>T
ENST00000673518.1:c.392C>T ENSP00000499889.1:p.Thr131Met
ENST00000673594.1:n.241C>T
ENST00000304874.13:c.392C>T ENSP00000307188.9:p.Thr131Met
ENST00000362000.9:c.197C>T ENSP00000354710.5:p.Thr66Met
ENST00000380839.8:c.392C>T ENSP00000370219.4:p.Thr131Met
ENST00000395331.3:c.392C>T ENSP00000378740.3:p.Thr131Met
ENST00000395332.7:c.392C>T ENSP00000378741.3:p.Thr131Met
ENST00000487982.5:n.458C>T
ENST00000496336.1:n.773C>T
NM_000048.3:c.392C>T NP_000039.2:p.Thr131Met
NM_001024943.1:c.392C>T NP_001020114.1:p.Thr131Met
NM_001024944.1:c.392C>T NP_001020115.1:p.Thr131Met
NM_001024946.1:c.392C>T NP_001020117.1:p.Thr131Met
NM_000048.4:c.392C>T MANE Select NP_000039.2:p.Thr131Met
NM_001024943.2:c.392C>T NP_001020114.1:p.Thr131Met
NM_001024944.2:c.392C>T NP_001020115.1:p.Thr131Met
NM_001024946.2:c.392C>T NP_001020117.1:p.Thr131Met