Canonical Allele Identifier: CA367645791

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554146G>T (hg19) ; chr7:g.66089159G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089159G>T , CM000669.2:g.66089159G>T	GRCh38
NC_000007.13:g.65554146G>T , CM000669.1:g.65554146G>T	GRCh37
NC_000007.12:g.65191581G>T	NCBI36
NG_009288.1:g.18371G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.902G>T MANE Select	ENSP00000307188.9:p.Gly301Val
ENST00000362000.10:c.707G>T	ENSP00000354710.6:p.Gly236Val
ENST00000380839.9:c.824G>T	ENSP00000370219.4:p.Gly275Val
ENST00000395331.4:c.902G>T	ENSP00000378740.3:p.Gly301Val
ENST00000395332.8:c.902G>T	ENSP00000378741.3:p.Gly301Val
ENST00000488343.2:c.71G>T	ENSP00000500864.1:p.Gly24Val
ENST00000671817.1:c.824G>T	ENSP00000500462.1:p.Gly275Val
ENST00000672498.1:c.*201G>T	ENSP00000500227.1:n.*201G>T
ENST00000672586.1:n.1661G>T
ENST00000672676.1:n.1926G>T
ENST00000673149.1:n.714G>T
ENST00000673350.1:n.3019G>T
ENST00000673518.1:c.824G>T	ENSP00000499889.1:p.Gly275Val
ENST00000304874.13:c.902G>T	ENSP00000307188.9:p.Gly301Val
ENST00000362000.9:c.707G>T	ENSP00000354710.5:p.Gly236Val
ENST00000380839.8:c.824G>T	ENSP00000370219.4:p.Gly275Val
ENST00000395331.3:c.902G>T	ENSP00000378740.3:p.Gly301Val
ENST00000395332.7:c.902G>T	ENSP00000378741.3:p.Gly301Val
ENST00000450043.2:c.215G>T	ENSP00000396527.2:p.Gly72Val
ENST00000488343.1:n.71G>T
ENST00000493708.5:n.283G>T
NM_000048.3:c.902G>T	NP_000039.2:p.Gly301Val
NM_001024943.1:c.902G>T	NP_001020114.1:p.Gly301Val
NM_001024944.1:c.902G>T	NP_001020115.1:p.Gly301Val
NM_001024946.1:c.824G>T	NP_001020117.1:p.Gly275Val
NM_000048.4:c.902G>T MANE Select	NP_000039.2:p.Gly301Val
NM_001024943.2:c.902G>T	NP_001020114.1:p.Gly301Val
NM_001024944.2:c.902G>T	NP_001020115.1:p.Gly301Val
NM_001024946.2:c.824G>T	NP_001020117.1:p.Gly275Val