Canonical Allele Identifier: CA1538676799

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998813G= , CM000667.2:g.34998813G=	GRCh38
NC_000005.9:g.34998918G= , CM000667.1:g.34998918G=	GRCh37
NC_000005.8:g.35034675G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1451C= MANE Select	ENSP00000231420.6:p.Ala484=
ENST00000231420.10:c.1451C=	ENSP00000231420.6:p.Ala484=
ENST00000510428.1:c.1226C=	ENSP00000422799.1:p.Ala409=
ENST00000512135.5:n.1121C=
ENST00000618015.4:c.1226C=	ENSP00000479154.1:p.Ala409=
NM_001306173.1:c.1226C=	NP_001293102.1:p.Ala409=
NM_031900.3:c.1451C=	NP_114106.1:p.Ala484=
XM_005248337.2:c.1448C=	XP_005248394.1:p.Ala483=
XM_005248338.2:c.1256C=	XP_005248395.1:p.Ala419=
XM_011514077.1:c.1438-411C=	XP_011512379.1:n.1438-411C=
XM_005248337.3:c.1448C=	XP_005248394.1:p.Ala483=
XM_005248338.3:c.1256C=	XP_005248395.1:p.Ala419=
XM_017009748.2:c.1226C=	XP_016865237.1:p.Ala409=
NM_031900.4:c.1451C= MANE Select	NP_114106.1:p.Ala484=
NM_001306173.2:c.1226C=	NP_001293102.1:p.Ala409=