Canonical Allele Identifier: CA1538676726
Gene: AGXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34998772C= , CM000667.2:g.34998772C= GRCh38
NC_000005.9:g.34998877C= , CM000667.1:g.34998877C= GRCh37
NC_000005.8:g.35034634C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231420.11:c.1492G= MANE Select ENSP00000231420.6:p.Val498=
ENST00000231420.10:c.1492G= ENSP00000231420.6:p.Val498=
ENST00000510428.1:c.1267G= ENSP00000422799.1:p.Val423=
ENST00000512135.5:n.1162G=
ENST00000618015.4:c.1267G= ENSP00000479154.1:p.Val423=
NM_001306173.1:c.1267G= NP_001293102.1:p.Val423=
NM_031900.3:c.1492G= NP_114106.1:p.Val498=
XM_005248337.2:c.1489G= XP_005248394.1:p.Val497=
XM_005248338.2:c.1297G= XP_005248395.1:p.Val433=
XM_011514077.1:c.1438-370G= XP_011512379.1:n.1438-370G=
XM_005248337.3:c.1489G= XP_005248394.1:p.Val497=
XM_005248338.3:c.1297G= XP_005248395.1:p.Val433=
XM_017009748.2:c.1267G= XP_016865237.1:p.Val423=
NM_031900.4:c.1492G= MANE Select NP_114106.1:p.Val498=
NM_001306173.2:c.1267G= NP_001293102.1:p.Val423=