Canonical Allele Identifier: CA455452980

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65557857G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66092870G>A , CM000669.2:g.66092870G>A	GRCh38
NC_000007.13:g.65557857G>A , CM000669.1:g.65557857G>A	GRCh37
NC_000007.12:g.65195292G>A	NCBI36
NG_009288.1:g.22082G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.1353G>A MANE Select	ENSP00000307188.9:p.Gln451=
ENST00000362000.10:c.1158G>A	ENSP00000354710.6:p.Gln386=
ENST00000380839.9:c.1275G>A	ENSP00000370219.4:p.Gln425=
ENST00000395331.4:c.1293G>A	ENSP00000378740.3:p.Gln431=
ENST00000395332.8:c.1353G>A	ENSP00000378741.3:p.Gln451=
ENST00000488343.2:c.148-34G>A	ENSP00000500864.1:n.148-34G>A
ENST00000672498.1:c.*756G>A	ENSP00000500227.1:n.*756G>A
ENST00000672586.1:n.2112G>A
ENST00000672676.1:n.2377G>A
ENST00000673149.1:n.1165G>A
ENST00000673350.1:n.3470G>A
ENST00000673518.1:c.1275G>A	ENSP00000499889.1:p.Gln425=
ENST00000304874.13:c.1353G>A	ENSP00000307188.9:p.Gln451=
ENST00000380839.8:c.1275G>A	ENSP00000370219.4:p.Gln425=
ENST00000395331.3:c.1293G>A	ENSP00000378740.3:p.Gln431=
ENST00000395332.7:c.1353G>A	ENSP00000378741.3:p.Gln451=
ENST00000450043.2:c.563+207G>A	ENSP00000396527.2:n.563+207G>A
ENST00000464970.1:n.556G>A
ENST00000488343.1:n.148-34G>A
ENST00000493708.5:n.834G>A
NM_000048.3:c.1353G>A	NP_000039.2:p.Gln451=
NM_001024943.1:c.1353G>A	NP_001020114.1:p.Gln451=
NM_001024944.1:c.1293G>A	NP_001020115.1:p.Gln431=
NM_001024946.1:c.1275G>A	NP_001020117.1:p.Gln425=
NM_000048.4:c.1353G>A MANE Select	NP_000039.2:p.Gln451=
NM_001024943.2:c.1353G>A	NP_001020114.1:p.Gln451=
NM_001024944.2:c.1293G>A	NP_001020115.1:p.Gln431=
NM_001024946.2:c.1275G>A	NP_001020117.1:p.Gln425=