Canonical Allele Identifier: CA1538676729
Gene: AGXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34998780T= , CM000667.2:g.34998780T= GRCh38
NC_000005.9:g.34998885T= , CM000667.1:g.34998885T= GRCh37
NC_000005.8:g.35034642T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231420.11:c.1484A= MANE Select ENSP00000231420.6:p.Asp495=
ENST00000231420.10:c.1484A= ENSP00000231420.6:p.Asp495=
ENST00000510428.1:c.1259A= ENSP00000422799.1:p.Asp420=
ENST00000512135.5:n.1154A=
ENST00000618015.4:c.1259A= ENSP00000479154.1:p.Asp420=
NM_001306173.1:c.1259A= NP_001293102.1:p.Asp420=
NM_031900.3:c.1484A= NP_114106.1:p.Asp495=
XM_005248337.2:c.1481A= XP_005248394.1:p.Asp494=
XM_005248338.2:c.1289A= XP_005248395.1:p.Asp430=
XM_011514077.1:c.1438-378A= XP_011512379.1:n.1438-378A=
XM_005248337.3:c.1481A= XP_005248394.1:p.Asp494=
XM_005248338.3:c.1289A= XP_005248395.1:p.Asp430=
XM_017009748.2:c.1259A= XP_016865237.1:p.Asp420=
NM_031900.4:c.1484A= MANE Select NP_114106.1:p.Asp495=
NM_001306173.2:c.1259A= NP_001293102.1:p.Asp420=