Canonical Allele Identifier: CA1713949113

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087282_66087284delinsGTC , CM000669.2:g.66087282_66087284delinsGTC	GRCh38
NC_000007.13:g.65552269_65552271delinsGTC , CM000669.1:g.65552269_65552271delinsGTC	GRCh37
NC_000007.12:g.65189704_65189706delinsGTC	NCBI36
NG_009288.1:g.16494_16496delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.603-52_603-50delinsGTC MANE Select	ENSP00000307188.9:n.603-52_603-50delinsGTC
ENST00000362000.10:c.408-52_408-50delinsGTC	ENSP00000354710.6:n.408-52_408-50delinsGTC
ENST00000380839.9:c.525-52_525-50delinsGTC	ENSP00000370219.4:n.525-52_525-50delinsGTC
ENST00000395331.4:c.603-52_603-50delinsGTC	ENSP00000378740.3:n.603-52_603-50delinsGTC
ENST00000395332.8:c.603-52_603-50delinsGTC	ENSP00000378741.3:n.603-52_603-50delinsGTC
ENST00000671817.1:c.525-52_525-50delinsGTC	ENSP00000500462.1:n.525-52_525-50delinsGTC
ENST00000672498.1:c.447-447_447-445delinsGTC	ENSP00000500227.1:n.447-447_447-445delinsGTC
ENST00000672586.1:n.968_970delinsGTC
ENST00000672676.1:n.1233_1235delinsGTC
ENST00000673149.1:n.415-52_415-50delinsGTC
ENST00000673350.1:n.1311_1313delinsGTC
ENST00000673518.1:c.525-52_525-50delinsGTC	ENSP00000499889.1:n.525-52_525-50delinsGTC
ENST00000673594.1:n.452-52_452-50delinsGTC
ENST00000304874.13:c.603-52_603-50delinsGTC	ENSP00000307188.9:n.603-52_603-50delinsGTC
ENST00000362000.9:c.408-52_408-50delinsGTC	ENSP00000354710.5:n.408-52_408-50delinsGTC
ENST00000380839.8:c.525-52_525-50delinsGTC	ENSP00000370219.4:n.525-52_525-50delinsGTC
ENST00000395331.3:c.603-52_603-50delinsGTC	ENSP00000378740.3:n.603-52_603-50delinsGTC
ENST00000395332.7:c.603-52_603-50delinsGTC	ENSP00000378741.3:n.603-52_603-50delinsGTC
NM_000048.3:c.603-52_603-50delinsGTC	NP_000039.2:n.603-52_603-50delinsGTC
NM_001024943.1:c.603-52_603-50delinsGTC	NP_001020114.1:n.603-52_603-50delinsGTC
NM_001024944.1:c.603-52_603-50delinsGTC	NP_001020115.1:n.603-52_603-50delinsGTC
NM_001024946.1:c.525-52_525-50delinsGTC	NP_001020117.1:n.525-52_525-50delinsGTC
NM_000048.4:c.603-52_603-50delinsGTC MANE Select	NP_000039.2:n.603-52_603-50delinsGTC
NM_001024943.2:c.603-52_603-50delinsGTC	NP_001020114.1:n.603-52_603-50delinsGTC
NM_001024944.2:c.603-52_603-50delinsGTC	NP_001020115.1:n.603-52_603-50delinsGTC
NM_001024946.2:c.525-52_525-50delinsGTC	NP_001020117.1:n.525-52_525-50delinsGTC