Canonical Allele Identifier: CA4276783

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66076051G>A , CM000669.2:g.66076051G>A	GRCh38
NC_000007.13:g.65541038G>A , CM000669.1:g.65541038G>A	GRCh37
NC_000007.12:g.65178473G>A	NCBI36
NG_009288.1:g.5263G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000048.4:c.-31G>A MANE Select	NP_000039.2:n.-31G>A
ENST00000304874.14:c.-31G>A MANE Select	ENSP00000307188.9:n.-31G>A
NM_000048.3:c.-31G>A	NP_000039.2:n.-31G>A
NM_001024943.1:c.-31G>A	NP_001020114.1:n.-31G>A
NM_001024943.2:c.-31G>A	NP_001020114.1:n.-31G>A
NM_001024944.1:c.-31G>A	NP_001020115.1:n.-31G>A
NM_001024944.2:c.-31G>A	NP_001020115.1:n.-31G>A
NM_001024946.1:c.-31G>A	NP_001020117.1:n.-31G>A
NM_001024946.2:c.-31G>A	NP_001020117.1:n.-31G>A
ENST00000304874.13:c.-31G>A	ENSP00000307188.9:n.-31G>A
ENST00000362000.10:c.-31G>A	ENSP00000354710.6:n.-31G>A
ENST00000362000.9:c.-31G>A	ENSP00000354710.5:n.-31G>A
ENST00000380839.8:c.-31G>A	ENSP00000370219.4:n.-31G>A
ENST00000380839.9:c.-31G>A	ENSP00000370219.4:n.-31G>A
ENST00000395331.3:c.-31G>A	ENSP00000378740.3:n.-31G>A
ENST00000395331.4:c.-31G>A	ENSP00000378740.3:n.-31G>A
ENST00000395332.7:c.-31G>A	ENSP00000378741.3:n.-31G>A
ENST00000395332.8:c.-31G>A	ENSP00000378741.3:n.-31G>A
ENST00000487982.5:n.36G>A
ENST00000496336.1:n.211G>A
ENST00000671817.1:c.-31G>A	ENSP00000500462.1:n.-31G>A
ENST00000672498.1:c.-31G>A	ENSP00000500227.1:n.-31G>A
ENST00000672586.1:n.70G>A
ENST00000672676.1:n.140G>A
ENST00000673350.1:n.218G>A
ENST00000673518.1:c.-31G>A	ENSP00000499889.1:n.-31G>A