Canonical Allele Identifier: CA4354466

Gene: ASNS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97852335C>G , CM000669.2:g.97852335C>G	GRCh38
NC_000007.13:g.97481647C>G , CM000669.1:g.97481647C>G	GRCh37
NC_000007.12:g.97319583C>G	NCBI36
NG_033870.1:g.25208G>C
NG_033870.2:g.81228G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001673.5:c.1610G>C MANE Select	NP_001664.3:p.Trp537Ser
ENST00000394308.8:c.1610G>C MANE Select	ENSP00000377845.3:p.Trp537Ser
NM_001178075.1:c.1547G>C	NP_001171546.1:p.Trp516Ser
NM_001178075.2:c.1547G>C	NP_001171546.1:p.Trp516Ser
NM_001178076.1:c.1361G>C	NP_001171547.1:p.Trp454Ser
NM_001178076.2:c.1361G>C	NP_001171547.1:p.Trp454Ser
NM_001178077.1:c.1361G>C	NP_001171548.1:p.Trp454Ser
NM_001352496.1:c.1610G>C	NP_001339425.1:p.Trp537Ser
NM_001352496.2:c.1610G>C	NP_001339425.1:p.Trp537Ser
NM_001673.4:c.1610G>C	NP_001664.3:p.Trp537Ser
NM_133436.3:c.1610G>C	NP_597680.2:p.Trp537Ser
NM_183356.3:c.1610G>C	NP_899199.2:p.Trp537Ser
NM_183356.4:c.1610G>C	NP_899199.2:p.Trp537Ser
NR_147989.1:n.3313G>C
ENST00000175506.8:c.1610G>C	ENSP00000175506.4:p.Trp537Ser
ENST00000394308.7:c.1610G>C	ENSP00000377845.3:p.Trp537Ser
ENST00000394309.7:c.1610G>C	ENSP00000377846.3:p.Trp537Ser
ENST00000422745.5:c.1547G>C	ENSP00000414901.1:p.Trp516Ser
ENST00000437628.5:c.1361G>C	ENSP00000414379.1:p.Trp454Ser
ENST00000444334.5:c.1547G>C	ENSP00000406994.1:p.Trp516Ser
ENST00000454046.5:c.*478G>C	ENSP00000401651.1:n.*478G>C
ENST00000455086.5:c.1361G>C	ENSP00000408472.1:p.Trp454Ser
ENST00000487714.1:n.668G>C