Canonical Allele Identifier: CA1713948497

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66086854_66086855delinsTG , CM000669.2:g.66086854_66086855delinsTG	GRCh38
NC_000007.13:g.65551841_65551842delinsTG , CM000669.1:g.65551841_65551842delinsTG	GRCh37
NC_000007.12:g.65189276_65189277delinsTG	NCBI36
NG_009288.1:g.16066_16067delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.602+33_602+34delinsTG MANE Select	ENSP00000307188.9:n.602+33_602+34delinsTG
ENST00000362000.10:c.407+33_407+34delinsTG	ENSP00000354710.6:n.407+33_407+34delinsTG
ENST00000380839.9:c.524+192_524+193delinsTG	ENSP00000370219.4:n.524+192_524+193delinsTG
ENST00000395331.4:c.602+33_602+34delinsTG	ENSP00000378740.3:n.602+33_602+34delinsTG
ENST00000395332.8:c.602+33_602+34delinsTG	ENSP00000378741.3:n.602+33_602+34delinsTG
ENST00000671817.1:c.524+192_524+193delinsTG	ENSP00000500462.1:n.524+192_524+193delinsTG
ENST00000672498.1:c.447-875_447-874delinsTG	ENSP00000500227.1:n.447-875_447-874delinsTG
ENST00000672586.1:n.540_541delinsTG
ENST00000672676.1:n.805_806delinsTG
ENST00000673149.1:n.414+33_414+34delinsTG
ENST00000673350.1:n.883_884delinsTG
ENST00000673518.1:c.524+192_524+193delinsTG	ENSP00000499889.1:n.524+192_524+193delinsTG
ENST00000673594.1:n.451+33_451+34delinsTG
ENST00000304874.13:c.602+33_602+34delinsTG	ENSP00000307188.9:n.602+33_602+34delinsTG
ENST00000362000.9:c.407+33_407+34delinsTG	ENSP00000354710.5:n.407+33_407+34delinsTG
ENST00000380839.8:c.524+192_524+193delinsTG	ENSP00000370219.4:n.524+192_524+193delinsTG
ENST00000395331.3:c.602+33_602+34delinsTG	ENSP00000378740.3:n.602+33_602+34delinsTG
ENST00000395332.7:c.602+33_602+34delinsTG	ENSP00000378741.3:n.602+33_602+34delinsTG
ENST00000487982.5:n.701_702delinsTG
NM_000048.3:c.602+33_602+34delinsTG	NP_000039.2:n.602+33_602+34delinsTG
NM_001024943.1:c.602+33_602+34delinsTG	NP_001020114.1:n.602+33_602+34delinsTG
NM_001024944.1:c.602+33_602+34delinsTG	NP_001020115.1:n.602+33_602+34delinsTG
NM_001024946.1:c.524+192_524+193delinsTG	NP_001020117.1:n.524+192_524+193delinsTG
NM_000048.4:c.602+33_602+34delinsTG MANE Select	NP_000039.2:n.602+33_602+34delinsTG
NM_001024943.2:c.602+33_602+34delinsTG	NP_001020114.1:n.602+33_602+34delinsTG
NM_001024944.2:c.602+33_602+34delinsTG	NP_001020115.1:n.602+33_602+34delinsTG
NM_001024946.2:c.524+192_524+193delinsTG	NP_001020117.1:n.524+192_524+193delinsTG