Canonical Allele Identifier: CA1713923696

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089291A= , CM000669.2:g.66089291A=	GRCh38
NC_000007.13:g.65554278A= , CM000669.1:g.65554278A=	GRCh37
NC_000007.12:g.65191713A=	NCBI36
NG_009288.1:g.18503A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.934A= MANE Select	ENSP00000307188.9:p.Met312=
ENST00000362000.10:c.739A=	ENSP00000354710.6:p.Met247=
ENST00000380839.9:c.856A=	ENSP00000370219.4:p.Met286=
ENST00000395331.4:c.918+116A=	ENSP00000378740.3:n.918+116A=
ENST00000395332.8:c.934A=	ENSP00000378741.3:p.Met312=
ENST00000488343.2:c.103A=	ENSP00000500864.1:p.Met35=
ENST00000671817.1:c.856A=	ENSP00000500462.1:p.Met286=
ENST00000672498.1:c.*233A=	ENSP00000500227.1:n.*233A=
ENST00000672586.1:n.1693A=
ENST00000672676.1:n.1958A=
ENST00000673149.1:n.746A=
ENST00000673350.1:n.3051A=
ENST00000673518.1:c.856A=	ENSP00000499889.1:p.Met286=
ENST00000304874.13:c.934A=	ENSP00000307188.9:p.Met312=
ENST00000380839.8:c.856A=	ENSP00000370219.4:p.Met286=
ENST00000395331.3:c.918+116A=	ENSP00000378740.3:n.918+116A=
ENST00000395332.7:c.934A=	ENSP00000378741.3:p.Met312=
ENST00000450043.2:c.247A=	ENSP00000396527.2:p.Met83=
ENST00000464970.1:n.53A=
ENST00000488343.1:n.103A=
ENST00000493708.5:n.415A=
NM_000048.3:c.934A=	NP_000039.2:p.Met312=
NM_001024943.1:c.934A=	NP_001020114.1:p.Met312=
NM_001024944.1:c.918+116A=	NP_001020115.1:n.918+116A=
NM_001024946.1:c.856A=	NP_001020117.1:p.Met286=
NM_000048.4:c.934A= MANE Select	NP_000039.2:p.Met312=
NM_001024943.2:c.934A=	NP_001020114.1:p.Met312=
NM_001024944.2:c.918+116A=	NP_001020115.1:n.918+116A=
NM_001024946.2:c.856A=	NP_001020117.1:p.Met286=