Canonical Allele Identifier: CA1538673395

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.35037010C= , CM000667.2:g.35037010C=	GRCh38
NC_000005.9:g.35037115C= , CM000667.1:g.35037115C=	GRCh37
NC_000005.8:g.35072872C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.418G= MANE Select	ENSP00000231420.6:p.Val140=
ENST00000231420.10:c.418G=	ENSP00000231420.6:p.Val140=
ENST00000505542.1:n.327G=
ENST00000510428.1:c.418G=	ENSP00000422799.1:p.Val140=
ENST00000618015.4:c.418G=	ENSP00000479154.1:p.Val140=
NM_001306173.1:c.418G=	NP_001293102.1:p.Val140=
NM_031900.3:c.418G=	NP_114106.1:p.Val140=
XM_005248337.2:c.415G=	XP_005248394.1:p.Val139=
XM_005248338.2:c.418G=	XP_005248395.1:p.Val140=
XM_011514077.1:c.418G=	XP_011512379.1:p.Val140=
XM_005248337.3:c.415G=	XP_005248394.1:p.Val139=
XM_005248338.3:c.418G=	XP_005248395.1:p.Val140=
XM_017009748.2:c.418G=	XP_016865237.1:p.Val140=
NM_031900.4:c.418G= MANE Select	NP_114106.1:p.Val140=
NM_001306173.2:c.418G=	NP_001293102.1:p.Val140=