Canonical Allele Identifier: CA367645877

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554158G>T (hg19) ; chr7:g.66089171G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089171G>T , CM000669.2:g.66089171G>T	GRCh38
NC_000007.13:g.65554158G>T , CM000669.1:g.65554158G>T	GRCh37
NC_000007.12:g.65191593G>T	NCBI36
NG_009288.1:g.18383G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.914G>T MANE Select	ENSP00000307188.9:p.Gly305Val
ENST00000362000.10:c.719G>T	ENSP00000354710.6:p.Gly240Val
ENST00000380839.9:c.836G>T	ENSP00000370219.4:p.Gly279Val
ENST00000395331.4:c.914G>T	ENSP00000378740.3:p.Gly305Val
ENST00000395332.8:c.914G>T	ENSP00000378741.3:p.Gly305Val
ENST00000488343.2:c.83G>T	ENSP00000500864.1:p.Gly28Val
ENST00000671817.1:c.836G>T	ENSP00000500462.1:p.Gly279Val
ENST00000672498.1:c.*213G>T	ENSP00000500227.1:n.*213G>T
ENST00000672586.1:n.1673G>T
ENST00000672676.1:n.1938G>T
ENST00000673149.1:n.726G>T
ENST00000673350.1:n.3031G>T
ENST00000673518.1:c.836G>T	ENSP00000499889.1:p.Gly279Val
ENST00000304874.13:c.914G>T	ENSP00000307188.9:p.Gly305Val
ENST00000362000.9:c.719G>T	ENSP00000354710.5:p.Gly240Val
ENST00000380839.8:c.836G>T	ENSP00000370219.4:p.Gly279Val
ENST00000395331.3:c.914G>T	ENSP00000378740.3:p.Gly305Val
ENST00000395332.7:c.914G>T	ENSP00000378741.3:p.Gly305Val
ENST00000450043.2:c.227G>T	ENSP00000396527.2:p.Gly76Val
ENST00000488343.1:n.83G>T
ENST00000493708.5:n.295G>T
NM_000048.3:c.914G>T	NP_000039.2:p.Gly305Val
NM_001024943.1:c.914G>T	NP_001020114.1:p.Gly305Val
NM_001024944.1:c.914G>T	NP_001020115.1:p.Gly305Val
NM_001024946.1:c.836G>T	NP_001020117.1:p.Gly279Val
NM_000048.4:c.914G>T MANE Select	NP_000039.2:p.Gly305Val
NM_001024943.2:c.914G>T	NP_001020114.1:p.Gly305Val
NM_001024944.2:c.914G>T	NP_001020115.1:p.Gly305Val
NM_001024946.2:c.836G>T	NP_001020117.1:p.Gly279Val