Canonical Allele Identifier: CA455680034

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554102G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089115G>A , CM000669.2:g.66089115G>A	GRCh38
NC_000007.13:g.65554102G>A , CM000669.1:g.65554102G>A	GRCh37
NC_000007.12:g.65191537G>A	NCBI36
NG_009288.1:g.18327G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.858G>A MANE Select	ENSP00000307188.9:p.Gln286=
ENST00000362000.10:c.663G>A	ENSP00000354710.6:p.Gln221=
ENST00000380839.9:c.780G>A	ENSP00000370219.4:p.Gln260=
ENST00000395331.4:c.858G>A	ENSP00000378740.3:p.Gln286=
ENST00000395332.8:c.858G>A	ENSP00000378741.3:p.Gln286=
ENST00000488343.2:c.27G>A	ENSP00000500864.1:p.Gln9=
ENST00000671817.1:c.780G>A	ENSP00000500462.1:p.Gln260=
ENST00000672498.1:c.*157G>A	ENSP00000500227.1:n.*157G>A
ENST00000672586.1:n.1617G>A
ENST00000672676.1:n.1882G>A
ENST00000673149.1:n.670G>A
ENST00000673350.1:n.2975G>A
ENST00000673518.1:c.780G>A	ENSP00000499889.1:p.Gln260=
ENST00000304874.13:c.858G>A	ENSP00000307188.9:p.Gln286=
ENST00000362000.9:c.663G>A	ENSP00000354710.5:p.Gln221=
ENST00000380839.8:c.780G>A	ENSP00000370219.4:p.Gln260=
ENST00000395331.3:c.858G>A	ENSP00000378740.3:p.Gln286=
ENST00000395332.7:c.858G>A	ENSP00000378741.3:p.Gln286=
ENST00000450043.2:c.171G>A	ENSP00000396527.2:p.Gln57=
ENST00000488343.1:n.27G>A
ENST00000493708.5:n.239G>A
NM_000048.3:c.858G>A	NP_000039.2:p.Gln286=
NM_001024943.1:c.858G>A	NP_001020114.1:p.Gln286=
NM_001024944.1:c.858G>A	NP_001020115.1:p.Gln286=
NM_001024946.1:c.780G>A	NP_001020117.1:p.Gln260=
NM_000048.4:c.858G>A MANE Select	NP_000039.2:p.Gln286=
NM_001024943.2:c.858G>A	NP_001020114.1:p.Gln286=
NM_001024944.2:c.858G>A	NP_001020115.1:p.Gln286=
NM_001024946.2:c.780G>A	NP_001020117.1:p.Gln260=