Canonical Allele Identifier: CA368265264

Gene: ASNS

Linked Data

• MyVariant Identifiers: chr7:g.97482679A>T (hg19) ; chr7:g.97853367A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97853367A>T , CM000669.2:g.97853367A>T	GRCh38
NC_000007.13:g.97482679A>T , CM000669.1:g.97482679A>T	GRCh37
NC_000007.12:g.97320615A>T	NCBI36
NG_033870.1:g.24176T>A
NG_033870.2:g.80196T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394308.8:c.1258T>A MANE Select	ENSP00000377845.3:p.Phe420Ile
ENST00000175506.8:c.1258T>A	ENSP00000175506.4:p.Phe420Ile
ENST00000394308.7:c.1258T>A	ENSP00000377845.3:p.Phe420Ile
ENST00000394309.7:c.1258T>A	ENSP00000377846.3:p.Phe420Ile
ENST00000422745.5:c.1195T>A	ENSP00000414901.1:p.Phe399Ile
ENST00000437628.5:c.1009T>A	ENSP00000414379.1:p.Phe337Ile
ENST00000444334.5:c.1195T>A	ENSP00000406994.1:p.Phe399Ile
ENST00000454046.5:c.*126T>A	ENSP00000401651.1:n.*126T>A
ENST00000455086.5:c.1009T>A	ENSP00000408472.1:p.Phe337Ile
ENST00000487714.1:n.316T>A
NM_001178075.1:c.1195T>A	NP_001171546.1:p.Phe399Ile
NM_001178076.1:c.1009T>A	NP_001171547.1:p.Phe337Ile
NM_001178077.1:c.1009T>A	NP_001171548.1:p.Phe337Ile
NM_001673.4:c.1258T>A	NP_001664.3:p.Phe420Ile
NM_133436.3:c.1258T>A	NP_597680.2:p.Phe420Ile
NM_183356.3:c.1258T>A	NP_899199.2:p.Phe420Ile
NM_001352496.1:c.1258T>A	NP_001339425.1:p.Phe420Ile
NR_147989.1:n.2961T>A
NM_001673.5:c.1258T>A MANE Select	NP_001664.3:p.Phe420Ile
NM_001178075.2:c.1195T>A	NP_001171546.1:p.Phe399Ile
NM_001178076.2:c.1009T>A	NP_001171547.1:p.Phe337Ile
NM_001352496.2:c.1258T>A	NP_001339425.1:p.Phe420Ile
NM_183356.4:c.1258T>A	NP_899199.2:p.Phe420Ile