Canonical Allele Identifier: CA368271293

Gene: ASNS

Linked Data

• MyVariant Identifiers: chr7:g.97493657A>C (hg19) ; chr7:g.97864345A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97864345A>C , CM000669.2:g.97864345A>C	GRCh38
NC_000007.13:g.97493657A>C , CM000669.1:g.97493657A>C	GRCh37
NC_000007.12:g.97331593A>C	NCBI36
NG_033870.1:g.13198T>G
NG_033870.2:g.69218T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394308.8:c.401T>G MANE Select	ENSP00000377845.3:p.Phe134Cys
ENST00000175506.8:c.401T>G	ENSP00000175506.4:p.Phe134Cys
ENST00000394308.7:c.401T>G	ENSP00000377845.3:p.Phe134Cys
ENST00000394309.7:c.401T>G	ENSP00000377846.3:p.Phe134Cys
ENST00000422745.5:c.338T>G	ENSP00000414901.1:p.Phe113Cys
ENST00000437628.5:c.152T>G	ENSP00000414379.1:p.Phe51Cys
ENST00000437657.5:c.401T>G	ENSP00000394242.1:p.Phe134Cys
ENST00000442734.5:c.401T>G	ENSP00000400422.1:p.Phe134Cys
ENST00000444334.5:c.338T>G	ENSP00000406994.1:p.Phe113Cys
ENST00000454046.5:c.401T>G	ENSP00000401651.1:p.Phe134Cys
ENST00000455086.5:c.152T>G	ENSP00000408472.1:p.Phe51Cys
ENST00000495255.1:n.429T>G
NM_001178075.1:c.338T>G	NP_001171546.1:p.Phe113Cys
NM_001178076.1:c.152T>G	NP_001171547.1:p.Phe51Cys
NM_001178077.1:c.152T>G	NP_001171548.1:p.Phe51Cys
NM_001673.4:c.401T>G	NP_001664.3:p.Phe134Cys
NM_133436.3:c.401T>G	NP_597680.2:p.Phe134Cys
NM_183356.3:c.401T>G	NP_899199.2:p.Phe134Cys
NM_001352496.1:c.401T>G	NP_001339425.1:p.Phe134Cys
NR_147989.1:n.2030T>G
NM_001673.5:c.401T>G MANE Select	NP_001664.3:p.Phe134Cys
NM_001178075.2:c.338T>G	NP_001171546.1:p.Phe113Cys
NM_001178076.2:c.152T>G	NP_001171547.1:p.Phe51Cys
NM_001352496.2:c.401T>G	NP_001339425.1:p.Phe134Cys
NM_183356.4:c.401T>G	NP_899199.2:p.Phe134Cys