Canonical Allele Identifier: CA2578899818

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66082504del , CM000669.2:g.66082504del	GRCh38
NC_000007.13:g.65547491del , CM000669.1:g.65547491del	GRCh37
NC_000007.12:g.65184926del	NCBI36
NG_009288.1:g.11716del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.291+53del MANE Select	ENSP00000307188.9:n.291+53del
ENST00000362000.10:c.96+53del	ENSP00000354710.6:n.96+53del
ENST00000380839.9:c.291+53del	ENSP00000370219.4:n.291+53del
ENST00000395331.4:c.291+53del	ENSP00000378740.3:n.291+53del
ENST00000395332.8:c.291+53del	ENSP00000378741.3:n.291+53del
ENST00000671817.1:c.291+53del	ENSP00000500462.1:n.291+53del
ENST00000672498.1:c.291+53del	ENSP00000500227.1:n.291+53del
ENST00000672586.1:n.196+53del
ENST00000672676.1:n.461+53del
ENST00000673350.1:n.539+53del
ENST00000673518.1:c.291+53del	ENSP00000499889.1:n.291+53del
ENST00000673594.1:n.140+53del
ENST00000304874.13:c.291+53del	ENSP00000307188.9:n.291+53del
ENST00000362000.9:c.96+53del	ENSP00000354710.5:n.96+53del
ENST00000380839.8:c.291+53del	ENSP00000370219.4:n.291+53del
ENST00000395331.3:c.291+53del	ENSP00000378740.3:n.291+53del
ENST00000395332.7:c.291+53del	ENSP00000378741.3:n.291+53del
ENST00000487982.5:n.357+53del
ENST00000496336.1:n.532+53del
NM_000048.3:c.291+53del	NP_000039.2:n.291+53del
NM_001024943.1:c.291+53del	NP_001020114.1:n.291+53del
NM_001024944.1:c.291+53del	NP_001020115.1:n.291+53del
NM_001024946.1:c.291+53del	NP_001020117.1:n.291+53del
NM_000048.4:c.291+53del MANE Select	NP_000039.2:n.291+53del
NM_001024943.2:c.291+53del	NP_001020114.1:n.291+53del
NM_001024944.2:c.291+53del	NP_001020115.1:n.291+53del
NM_001024946.2:c.291+53del	NP_001020117.1:n.291+53del