Canonical Allele Identifier: CA1538676792

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998812C= , CM000667.2:g.34998812C=	GRCh38
NC_000005.9:g.34998917C= , CM000667.1:g.34998917C=	GRCh37
NC_000005.8:g.35034674C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1452G= MANE Select	ENSP00000231420.6:p.Ala484=
ENST00000231420.10:c.1452G=	ENSP00000231420.6:p.Ala484=
ENST00000510428.1:c.1227G=	ENSP00000422799.1:p.Ala409=
ENST00000512135.5:n.1122G=
ENST00000618015.4:c.1227G=	ENSP00000479154.1:p.Ala409=
NM_001306173.1:c.1227G=	NP_001293102.1:p.Ala409=
NM_031900.3:c.1452G=	NP_114106.1:p.Ala484=
XM_005248337.2:c.1449G=	XP_005248394.1:p.Ala483=
XM_005248338.2:c.1257G=	XP_005248395.1:p.Ala419=
XM_011514077.1:c.1438-410G=	XP_011512379.1:n.1438-410G=
XM_005248337.3:c.1449G=	XP_005248394.1:p.Ala483=
XM_005248338.3:c.1257G=	XP_005248395.1:p.Ala419=
XM_017009748.2:c.1227G=	XP_016865237.1:p.Ala409=
NM_031900.4:c.1452G= MANE Select	NP_114106.1:p.Ala484=
NM_001306173.2:c.1227G=	NP_001293102.1:p.Ala409=