Canonical Allele Identifier: CA1538676484

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998598A= , CM000667.2:g.34998598A=	GRCh38
NC_000005.9:g.34998703A= , CM000667.1:g.34998703A=	GRCh37
NC_000005.8:g.35034460A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.*121T= MANE Select	ENSP00000231420.6:n.*121T=
ENST00000231420.10:c.*121T=	ENSP00000231420.6:n.*121T=
ENST00000510428.1:c.*45+76T=	ENSP00000422799.1:n.*45+76T=
ENST00000512135.5:n.1336T=
ENST00000618015.4:c.*121T=	ENSP00000479154.1:n.*121T=
NM_001306173.1:c.*45+76T=	NP_001293102.1:n.*45+76T=
NM_031900.3:c.*121T=	NP_114106.1:n.*121T=
XM_005248337.2:c.*121T=	XP_005248394.1:n.*121T=
XM_005248338.2:c.*121T=	XP_005248395.1:n.*121T=
XM_011514077.1:c.1438-196T=	XP_011512379.1:n.1438-196T=
XM_005248337.3:c.*121T=	XP_005248394.1:n.*121T=
XM_005248338.3:c.*121T=	XP_005248395.1:n.*121T=
XM_017009748.2:c.*121T=	XP_016865237.1:n.*121T=
NM_031900.4:c.*121T= MANE Select	NP_114106.1:n.*121T=
NM_001306173.2:c.*45+76T=	NP_001293102.1:n.*45+76T=