Canonical Allele Identifier: CA1713928836
Gene: ASL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66092772_66092773delinsCT , CM000669.2:g.66092772_66092773delinsCT GRCh38
NC_000007.13:g.65557759_65557760delinsCT , CM000669.1:g.65557759_65557760delinsCT GRCh37
NC_000007.12:g.65195194_65195195delinsCT NCBI36
NG_009288.1:g.21984_21985delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000304874.14:c.1255_1256delinsCT MANE Select ENSP00000307188.9:p.Leu419=
ENST00000362000.10:c.1060_1061delinsCT ENSP00000354710.6:p.Leu354=
ENST00000380839.9:c.1177_1178delinsCT ENSP00000370219.4:p.Leu393=
ENST00000395331.4:c.1195_1196delinsCT ENSP00000378740.3:p.Leu399=
ENST00000395332.8:c.1255_1256delinsCT ENSP00000378741.3:p.Leu419=
ENST00000488343.2:c.148-132_148-131delinsCT ENSP00000500864.1:n.148-132_148-131delinsCT
ENST00000672498.1:c.*658_*659delinsCT ENSP00000500227.1:n.*658_*659delinsCT
ENST00000672586.1:n.2014_2015delinsCT
ENST00000672676.1:n.2279_2280delinsCT
ENST00000673149.1:n.1067_1068delinsCT
ENST00000673350.1:n.3372_3373delinsCT
ENST00000673518.1:c.1177_1178delinsCT ENSP00000499889.1:p.Leu393=
ENST00000304874.13:c.1255_1256delinsCT ENSP00000307188.9:p.Leu419=
ENST00000380839.8:c.1177_1178delinsCT ENSP00000370219.4:p.Leu393=
ENST00000395331.3:c.1195_1196delinsCT ENSP00000378740.3:p.Leu399=
ENST00000395332.7:c.1255_1256delinsCT ENSP00000378741.3:p.Leu419=
ENST00000450043.2:c.563+109_563+110delinsCT ENSP00000396527.2:n.563+109_563+110delinsCT
ENST00000464970.1:n.458_459delinsCT
ENST00000488343.1:n.148-132_148-131delinsCT
ENST00000493708.5:n.736_737delinsCT
NM_000048.3:c.1255_1256delinsCT NP_000039.2:p.Leu419=
NM_001024943.1:c.1255_1256delinsCT NP_001020114.1:p.Leu419=
NM_001024944.1:c.1195_1196delinsCT NP_001020115.1:p.Leu399=
NM_001024946.1:c.1177_1178delinsCT NP_001020117.1:p.Leu393=
NM_000048.4:c.1255_1256delinsCT MANE Select NP_000039.2:p.Leu419=
NM_001024943.2:c.1255_1256delinsCT NP_001020114.1:p.Leu419=
NM_001024944.2:c.1195_1196delinsCT NP_001020115.1:p.Leu399=
NM_001024946.2:c.1177_1178delinsCT NP_001020117.1:p.Leu393=