Canonical Allele Identifier: CA1713923278

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089132G= , CM000669.2:g.66089132G=	GRCh38
NC_000007.13:g.65554119G= , CM000669.1:g.65554119G=	GRCh37
NC_000007.12:g.65191554G=	NCBI36
NG_009288.1:g.18344G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.875G= MANE Select	ENSP00000307188.9:p.Ser292=
ENST00000362000.10:c.680G=	ENSP00000354710.6:p.Ser227=
ENST00000380839.9:c.797G=	ENSP00000370219.4:p.Ser266=
ENST00000395331.4:c.875G=	ENSP00000378740.3:p.Ser292=
ENST00000395332.8:c.875G=	ENSP00000378741.3:p.Ser292=
ENST00000488343.2:c.44G=	ENSP00000500864.1:p.Ser15=
ENST00000671817.1:c.797G=	ENSP00000500462.1:p.Ser266=
ENST00000672498.1:c.*174G=	ENSP00000500227.1:n.*174G=
ENST00000672586.1:n.1634G=
ENST00000672676.1:n.1899G=
ENST00000673149.1:n.687G=
ENST00000673350.1:n.2992G=
ENST00000673518.1:c.797G=	ENSP00000499889.1:p.Ser266=
ENST00000304874.13:c.875G=	ENSP00000307188.9:p.Ser292=
ENST00000362000.9:c.680G=	ENSP00000354710.5:p.Ser227=
ENST00000380839.8:c.797G=	ENSP00000370219.4:p.Ser266=
ENST00000395331.3:c.875G=	ENSP00000378740.3:p.Ser292=
ENST00000395332.7:c.875G=	ENSP00000378741.3:p.Ser292=
ENST00000450043.2:c.188G=	ENSP00000396527.2:p.Ser63=
ENST00000488343.1:n.44G=
ENST00000493708.5:n.256G=
NM_000048.3:c.875G=	NP_000039.2:p.Ser292=
NM_001024943.1:c.875G=	NP_001020114.1:p.Ser292=
NM_001024944.1:c.875G=	NP_001020115.1:p.Ser292=
NM_001024946.1:c.797G=	NP_001020117.1:p.Ser266=
NM_000048.4:c.875G= MANE Select	NP_000039.2:p.Ser292=
NM_001024943.2:c.875G=	NP_001020114.1:p.Ser292=
NM_001024944.2:c.875G=	NP_001020115.1:p.Ser292=
NM_001024946.2:c.797G=	NP_001020117.1:p.Ser266=