Canonical Allele Identifier: CA368264188

Gene: ASNS

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97852375G>T , CM000669.2:g.97852375G>T	GRCh38
NC_000007.13:g.97481687G>T , CM000669.1:g.97481687G>T	GRCh37
NC_000007.12:g.97319623G>T	NCBI36
NG_033870.1:g.25168C>A
NG_033870.2:g.81188C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394308.8:c.1570C>A MANE Select	ENSP00000377845.3:p.Arg524Ser
ENST00000175506.8:c.1570C>A	ENSP00000175506.4:p.Arg524Ser
ENST00000394308.7:c.1570C>A	ENSP00000377845.3:p.Arg524Ser
ENST00000394309.7:c.1570C>A	ENSP00000377846.3:p.Arg524Ser
ENST00000422745.5:c.1507C>A	ENSP00000414901.1:p.Arg503Ser
ENST00000437628.5:c.1321C>A	ENSP00000414379.1:p.Arg441Ser
ENST00000444334.5:c.1507C>A	ENSP00000406994.1:p.Arg503Ser
ENST00000454046.5:c.*438C>A	ENSP00000401651.1:n.*438C>A
ENST00000455086.5:c.1321C>A	ENSP00000408472.1:p.Arg441Ser
ENST00000487714.1:n.628C>A
NM_001178075.1:c.1507C>A	NP_001171546.1:p.Arg503Ser
NM_001178076.1:c.1321C>A	NP_001171547.1:p.Arg441Ser
NM_001178077.1:c.1321C>A	NP_001171548.1:p.Arg441Ser
NM_001673.4:c.1570C>A	NP_001664.3:p.Arg524Ser
NM_133436.3:c.1570C>A	NP_597680.2:p.Arg524Ser
NM_183356.3:c.1570C>A	NP_899199.2:p.Arg524Ser
NM_001352496.1:c.1570C>A	NP_001339425.1:p.Arg524Ser
NR_147989.1:n.3273C>A
NM_001673.5:c.1570C>A MANE Select	NP_001664.3:p.Arg524Ser
NM_001178075.2:c.1507C>A	NP_001171546.1:p.Arg503Ser
NM_001178076.2:c.1321C>A	NP_001171547.1:p.Arg441Ser
NM_001352496.2:c.1570C>A	NP_001339425.1:p.Arg524Ser
NM_183356.4:c.1570C>A	NP_899199.2:p.Arg524Ser