Canonical Allele Identifier: CA159933464

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66088810A>C , CM000669.2:g.66088810A>C	GRCh38
NC_000007.13:g.65553797A>C , CM000669.1:g.65553797A>C	GRCh37
NC_000007.12:g.65191232A>C	NCBI36
NG_009288.1:g.18022A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000048.4:c.722A>C MANE Select	NP_000039.2:p.Glu241Ala
ENST00000304874.14:c.722A>C MANE Select	ENSP00000307188.9:p.Glu241Ala
NM_000048.3:c.722A>C	NP_000039.2:p.Glu241Ala
NM_001024943.1:c.722A>C	NP_001020114.1:p.Glu241Ala
NM_001024943.2:c.722A>C	NP_001020114.1:p.Glu241Ala
NM_001024944.1:c.722A>C	NP_001020115.1:p.Glu241Ala
NM_001024944.2:c.722A>C	NP_001020115.1:p.Glu241Ala
NM_001024946.1:c.644A>C	NP_001020117.1:p.Glu215Ala
NM_001024946.2:c.644A>C	NP_001020117.1:p.Glu215Ala
ENST00000304874.13:c.722A>C	ENSP00000307188.9:p.Glu241Ala
ENST00000362000.10:c.527A>C	ENSP00000354710.6:p.Glu176Ala
ENST00000362000.9:c.527A>C	ENSP00000354710.5:p.Glu176Ala
ENST00000380839.8:c.644A>C	ENSP00000370219.4:p.Glu215Ala
ENST00000380839.9:c.644A>C	ENSP00000370219.4:p.Glu215Ala
ENST00000395331.3:c.722A>C	ENSP00000378740.3:p.Glu241Ala
ENST00000395331.4:c.722A>C	ENSP00000378740.3:p.Glu241Ala
ENST00000395332.7:c.722A>C	ENSP00000378741.3:p.Glu241Ala
ENST00000395332.8:c.722A>C	ENSP00000378741.3:p.Glu241Ala
ENST00000450043.2:c.35A>C	ENSP00000396527.2:p.Glu12Ala
ENST00000493708.5:n.103A>C
ENST00000671817.1:c.644A>C	ENSP00000500462.1:p.Glu215Ala
ENST00000672498.1:c.*21A>C	ENSP00000500227.1:n.*21A>C
ENST00000672586.1:n.1481A>C
ENST00000672676.1:n.1746A>C
ENST00000673149.1:n.534A>C
ENST00000673350.1:n.2839A>C
ENST00000673518.1:c.644A>C	ENSP00000499889.1:p.Glu215Ala