Canonical Allele Identifier: CA4354796

Gene: ASNS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97864458C>T , CM000669.2:g.97864458C>T	GRCh38
NC_000007.13:g.97493770C>T , CM000669.1:g.97493770C>T	GRCh37
NC_000007.12:g.97331706C>T	NCBI36
NG_033870.1:g.13085G>A
NG_033870.2:g.69105G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394308.8:c.288G>A MANE Select	ENSP00000377845.3:p.Val96=
ENST00000175506.8:c.288G>A	ENSP00000175506.4:p.Val96=
ENST00000394308.7:c.288G>A	ENSP00000377845.3:p.Val96=
ENST00000394309.7:c.288G>A	ENSP00000377846.3:p.Val96=
ENST00000422745.5:c.225G>A	ENSP00000414901.1:p.Val75=
ENST00000437628.5:c.39G>A	ENSP00000414379.1:p.Val13=
ENST00000437657.5:c.288G>A	ENSP00000394242.1:p.Val96=
ENST00000442734.5:c.288G>A	ENSP00000400422.1:p.Val96=
ENST00000444334.5:c.225G>A	ENSP00000406994.1:p.Val75=
ENST00000448127.1:c.288G>A	ENSP00000402350.1:p.Val96=
ENST00000454046.5:c.288G>A	ENSP00000401651.1:p.Val96=
ENST00000455086.5:c.39G>A	ENSP00000408472.1:p.Val13=
ENST00000495255.1:n.316G>A
NM_001178075.1:c.225G>A	NP_001171546.1:p.Val75=
NM_001178076.1:c.39G>A	NP_001171547.1:p.Val13=
NM_001178077.1:c.39G>A	NP_001171548.1:p.Val13=
NM_001673.4:c.288G>A	NP_001664.3:p.Val96=
NM_133436.3:c.288G>A	NP_597680.2:p.Val96=
NM_183356.3:c.288G>A	NP_899199.2:p.Val96=
NM_001352496.1:c.288G>A	NP_001339425.1:p.Val96=
NR_147989.1:n.1917G>A
NM_001673.5:c.288G>A MANE Select	NP_001664.3:p.Val96=
NM_001178075.2:c.225G>A	NP_001171546.1:p.Val75=
NM_001178076.2:c.39G>A	NP_001171547.1:p.Val13=
NM_001352496.2:c.288G>A	NP_001339425.1:p.Val96=
NM_183356.4:c.288G>A	NP_899199.2:p.Val96=