Canonical Allele Identifier: CA1713948088

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66086716_66086717delinsTG , CM000669.2:g.66086716_66086717delinsTG	GRCh38
NC_000007.13:g.65551703_65551704delinsTG , CM000669.1:g.65551703_65551704delinsTG	GRCh37
NC_000007.12:g.65189138_65189139delinsTG	NCBI36
NG_009288.1:g.15928_15929delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.525-28_525-27delinsTG MANE Select	ENSP00000307188.9:n.525-28_525-27delinsTG
ENST00000362000.10:c.330-28_330-27delinsTG	ENSP00000354710.6:n.330-28_330-27delinsTG
ENST00000380839.9:c.524+54_524+55delinsTG	ENSP00000370219.4:n.524+54_524+55delinsTG
ENST00000395331.4:c.525-28_525-27delinsTG	ENSP00000378740.3:n.525-28_525-27delinsTG
ENST00000395332.8:c.525-28_525-27delinsTG	ENSP00000378741.3:n.525-28_525-27delinsTG
ENST00000671817.1:c.524+54_524+55delinsTG	ENSP00000500462.1:n.524+54_524+55delinsTG
ENST00000672498.1:c.447-1013_447-1012delinsTG	ENSP00000500227.1:n.447-1013_447-1012delinsTG
ENST00000672586.1:n.430-28_430-27delinsTG
ENST00000672676.1:n.695-28_695-27delinsTG
ENST00000673149.1:n.337-28_337-27delinsTG
ENST00000673350.1:n.773-28_773-27delinsTG
ENST00000673518.1:c.524+54_524+55delinsTG	ENSP00000499889.1:n.524+54_524+55delinsTG
ENST00000673594.1:n.374-28_374-27delinsTG
ENST00000304874.13:c.525-28_525-27delinsTG	ENSP00000307188.9:n.525-28_525-27delinsTG
ENST00000362000.9:c.330-28_330-27delinsTG	ENSP00000354710.5:n.330-28_330-27delinsTG
ENST00000380839.8:c.524+54_524+55delinsTG	ENSP00000370219.4:n.524+54_524+55delinsTG
ENST00000395331.3:c.525-28_525-27delinsTG	ENSP00000378740.3:n.525-28_525-27delinsTG
ENST00000395332.7:c.525-28_525-27delinsTG	ENSP00000378741.3:n.525-28_525-27delinsTG
ENST00000487982.5:n.591-28_591-27delinsTG
NM_000048.3:c.525-28_525-27delinsTG	NP_000039.2:n.525-28_525-27delinsTG
NM_001024943.1:c.525-28_525-27delinsTG	NP_001020114.1:n.525-28_525-27delinsTG
NM_001024944.1:c.525-28_525-27delinsTG	NP_001020115.1:n.525-28_525-27delinsTG
NM_001024946.1:c.524+54_524+55delinsTG	NP_001020117.1:n.524+54_524+55delinsTG
NM_000048.4:c.525-28_525-27delinsTG MANE Select	NP_000039.2:n.525-28_525-27delinsTG
NM_001024943.2:c.525-28_525-27delinsTG	NP_001020114.1:n.525-28_525-27delinsTG
NM_001024944.2:c.525-28_525-27delinsTG	NP_001020115.1:n.525-28_525-27delinsTG
NM_001024946.2:c.524+54_524+55delinsTG	NP_001020117.1:n.524+54_524+55delinsTG