Canonical Allele Identifier: CA367644411

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65552725T>A (hg19) ; chr7:g.66087738T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087738T>A , CM000669.2:g.66087738T>A	GRCh38
NC_000007.13:g.65552725T>A , CM000669.1:g.65552725T>A	GRCh37
NC_000007.12:g.65190160T>A	NCBI36
NG_009288.1:g.16950T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.665T>A MANE Select	ENSP00000307188.9:p.Phe222Tyr
ENST00000362000.10:c.470T>A	ENSP00000354710.6:p.Phe157Tyr
ENST00000380839.9:c.587T>A	ENSP00000370219.4:p.Phe196Tyr
ENST00000395331.4:c.665T>A	ENSP00000378740.3:p.Phe222Tyr
ENST00000395332.8:c.665T>A	ENSP00000378741.3:p.Phe222Tyr
ENST00000671817.1:c.587T>A	ENSP00000500462.1:p.Phe196Tyr
ENST00000672498.1:c.456T>A	ENSP00000500227.1:p.Leu152=
ENST00000672586.1:n.1424T>A
ENST00000672676.1:n.1689T>A
ENST00000673149.1:n.477T>A
ENST00000673350.1:n.1767T>A
ENST00000673518.1:c.587T>A	ENSP00000499889.1:p.Phe196Tyr
ENST00000304874.13:c.665T>A	ENSP00000307188.9:p.Phe222Tyr
ENST00000362000.9:c.470T>A	ENSP00000354710.5:p.Phe157Tyr
ENST00000380839.8:c.587T>A	ENSP00000370219.4:p.Phe196Tyr
ENST00000395331.3:c.665T>A	ENSP00000378740.3:p.Phe222Tyr
ENST00000395332.7:c.665T>A	ENSP00000378741.3:p.Phe222Tyr
ENST00000493708.5:n.46T>A
NM_000048.3:c.665T>A	NP_000039.2:p.Phe222Tyr
NM_001024943.1:c.665T>A	NP_001020114.1:p.Phe222Tyr
NM_001024944.1:c.665T>A	NP_001020115.1:p.Phe222Tyr
NM_001024946.1:c.587T>A	NP_001020117.1:p.Phe196Tyr
NM_000048.4:c.665T>A MANE Select	NP_000039.2:p.Phe222Tyr
NM_001024943.2:c.665T>A	NP_001020114.1:p.Phe222Tyr
NM_001024944.2:c.665T>A	NP_001020115.1:p.Phe222Tyr
NM_001024946.2:c.587T>A	NP_001020117.1:p.Phe196Tyr