Canonical Allele Identifier: CA1713949118

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087283_66087286delinsTCAG , CM000669.2:g.66087283_66087286delinsTCAG	GRCh38
NC_000007.13:g.65552270_65552273delinsTCAG , CM000669.1:g.65552270_65552273delinsTCAG	GRCh37
NC_000007.12:g.65189705_65189708delinsTCAG	NCBI36
NG_009288.1:g.16495_16498delinsTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.603-51_603-48delinsTCAG MANE Select	ENSP00000307188.9:n.603-51_603-48delinsTCAG
ENST00000362000.10:c.408-51_408-48delinsTCAG	ENSP00000354710.6:n.408-51_408-48delinsTCAG
ENST00000380839.9:c.525-51_525-48delinsTCAG	ENSP00000370219.4:n.525-51_525-48delinsTCAG
ENST00000395331.4:c.603-51_603-48delinsTCAG	ENSP00000378740.3:n.603-51_603-48delinsTCAG
ENST00000395332.8:c.603-51_603-48delinsTCAG	ENSP00000378741.3:n.603-51_603-48delinsTCAG
ENST00000671817.1:c.525-51_525-48delinsTCAG	ENSP00000500462.1:n.525-51_525-48delinsTCAG
ENST00000672498.1:c.447-446_447-443delinsTCAG	ENSP00000500227.1:n.447-446_447-443delinsTCAG
ENST00000672586.1:n.969_972delinsTCAG
ENST00000672676.1:n.1234_1237delinsTCAG
ENST00000673149.1:n.415-51_415-48delinsTCAG
ENST00000673350.1:n.1312_1315delinsTCAG
ENST00000673518.1:c.525-51_525-48delinsTCAG	ENSP00000499889.1:n.525-51_525-48delinsTCAG
ENST00000673594.1:n.452-51_452-48delinsTCAG
ENST00000304874.13:c.603-51_603-48delinsTCAG	ENSP00000307188.9:n.603-51_603-48delinsTCAG
ENST00000362000.9:c.408-51_408-48delinsTCAG	ENSP00000354710.5:n.408-51_408-48delinsTCAG
ENST00000380839.8:c.525-51_525-48delinsTCAG	ENSP00000370219.4:n.525-51_525-48delinsTCAG
ENST00000395331.3:c.603-51_603-48delinsTCAG	ENSP00000378740.3:n.603-51_603-48delinsTCAG
ENST00000395332.7:c.603-51_603-48delinsTCAG	ENSP00000378741.3:n.603-51_603-48delinsTCAG
NM_000048.3:c.603-51_603-48delinsTCAG	NP_000039.2:n.603-51_603-48delinsTCAG
NM_001024943.1:c.603-51_603-48delinsTCAG	NP_001020114.1:n.603-51_603-48delinsTCAG
NM_001024944.1:c.603-51_603-48delinsTCAG	NP_001020115.1:n.603-51_603-48delinsTCAG
NM_001024946.1:c.525-51_525-48delinsTCAG	NP_001020117.1:n.525-51_525-48delinsTCAG
NM_000048.4:c.603-51_603-48delinsTCAG MANE Select	NP_000039.2:n.603-51_603-48delinsTCAG
NM_001024943.2:c.603-51_603-48delinsTCAG	NP_001020114.1:n.603-51_603-48delinsTCAG
NM_001024944.2:c.603-51_603-48delinsTCAG	NP_001020115.1:n.603-51_603-48delinsTCAG
NM_001024946.2:c.525-51_525-48delinsTCAG	NP_001020117.1:n.525-51_525-48delinsTCAG