Canonical Allele Identifier: CA367646572
Gene: ASL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66089324A>T , CM000669.2:g.66089324A>T GRCh38
NC_000007.13:g.65554311A>T , CM000669.1:g.65554311A>T GRCh37
NC_000007.12:g.65191746A>T NCBI36
NG_009288.1:g.18536A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304874.14:c.967A>T MANE Select ENSP00000307188.9:p.Lys323Ter
ENST00000362000.10:c.772A>T ENSP00000354710.6:p.Lys258Ter
ENST00000380839.9:c.889A>T ENSP00000370219.4:p.Lys297Ter
ENST00000395331.4:c.918+149A>T ENSP00000378740.3:n.918+149A>T
ENST00000395332.8:c.967A>T ENSP00000378741.3:p.Lys323Ter
ENST00000488343.2:c.136A>T ENSP00000500864.1:p.Lys46Ter
ENST00000671817.1:c.889A>T ENSP00000500462.1:p.Lys297Ter
ENST00000672498.1:c.*266A>T ENSP00000500227.1:n.*266A>T
ENST00000672586.1:n.1726A>T
ENST00000672676.1:n.1991A>T
ENST00000673149.1:n.779A>T
ENST00000673350.1:n.3084A>T
ENST00000673518.1:c.889A>T ENSP00000499889.1:p.Lys297Ter
ENST00000304874.13:c.967A>T ENSP00000307188.9:p.Lys323Ter
ENST00000380839.8:c.889A>T ENSP00000370219.4:p.Lys297Ter
ENST00000395331.3:c.918+149A>T ENSP00000378740.3:n.918+149A>T
ENST00000395332.7:c.967A>T ENSP00000378741.3:p.Lys323Ter
ENST00000450043.2:c.280A>T ENSP00000396527.2:p.Lys94Ter
ENST00000464970.1:n.86A>T
ENST00000488343.1:n.136A>T
ENST00000493708.5:n.448A>T
NM_000048.3:c.967A>T NP_000039.2:p.Lys323Ter
NM_001024943.1:c.967A>T NP_001020114.1:p.Lys323Ter
NM_001024944.1:c.918+149A>T NP_001020115.1:n.918+149A>T
NM_001024946.1:c.889A>T NP_001020117.1:p.Lys297Ter
NM_000048.4:c.967A>T MANE Select NP_000039.2:p.Lys323Ter
NM_001024943.2:c.967A>T NP_001020114.1:p.Lys323Ter
NM_001024944.2:c.918+149A>T NP_001020115.1:n.918+149A>T
NM_001024946.2:c.889A>T NP_001020117.1:p.Lys297Ter