Canonical Allele Identifier: CA367645087

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66088809G>A , CM000669.2:g.66088809G>A	GRCh38
NC_000007.13:g.65553796G>A , CM000669.1:g.65553796G>A	GRCh37
NC_000007.12:g.65191231G>A	NCBI36
NG_009288.1:g.18021G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000048.4:c.721G>A MANE Select	NP_000039.2:p.Glu241Lys
ENST00000304874.14:c.721G>A MANE Select	ENSP00000307188.9:p.Glu241Lys
NM_000048.3:c.721G>A	NP_000039.2:p.Glu241Lys
NM_001024943.1:c.721G>A	NP_001020114.1:p.Glu241Lys
NM_001024943.2:c.721G>A	NP_001020114.1:p.Glu241Lys
NM_001024944.1:c.721G>A	NP_001020115.1:p.Glu241Lys
NM_001024944.2:c.721G>A	NP_001020115.1:p.Glu241Lys
NM_001024946.1:c.643G>A	NP_001020117.1:p.Glu215Lys
NM_001024946.2:c.643G>A	NP_001020117.1:p.Glu215Lys
ENST00000304874.13:c.721G>A	ENSP00000307188.9:p.Glu241Lys
ENST00000362000.10:c.526G>A	ENSP00000354710.6:p.Glu176Lys
ENST00000362000.9:c.526G>A	ENSP00000354710.5:p.Glu176Lys
ENST00000380839.8:c.643G>A	ENSP00000370219.4:p.Glu215Lys
ENST00000380839.9:c.643G>A	ENSP00000370219.4:p.Glu215Lys
ENST00000395331.3:c.721G>A	ENSP00000378740.3:p.Glu241Lys
ENST00000395331.4:c.721G>A	ENSP00000378740.3:p.Glu241Lys
ENST00000395332.7:c.721G>A	ENSP00000378741.3:p.Glu241Lys
ENST00000395332.8:c.721G>A	ENSP00000378741.3:p.Glu241Lys
ENST00000450043.2:c.34G>A	ENSP00000396527.2:p.Glu12Lys
ENST00000493708.5:n.102G>A
ENST00000671817.1:c.643G>A	ENSP00000500462.1:p.Glu215Lys
ENST00000672498.1:c.*20G>A	ENSP00000500227.1:n.*20G>A
ENST00000672586.1:n.1480G>A
ENST00000672676.1:n.1745G>A
ENST00000673149.1:n.533G>A
ENST00000673350.1:n.2838G>A
ENST00000673518.1:c.643G>A	ENSP00000499889.1:p.Glu215Lys