Canonical Allele Identifier: CA1538676447

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998577G= , CM000667.2:g.34998577G=	GRCh38
NC_000005.9:g.34998682G= , CM000667.1:g.34998682G=	GRCh37
NC_000005.8:g.35034439G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.*142C= MANE Select	ENSP00000231420.6:n.*142C=
ENST00000231420.10:c.*142C=	ENSP00000231420.6:n.*142C=
ENST00000510428.1:c.*45+97C=	ENSP00000422799.1:n.*45+97C=
ENST00000512135.5:n.1357C=
ENST00000618015.4:c.*142C=	ENSP00000479154.1:n.*142C=
NM_001306173.1:c.*45+97C=	NP_001293102.1:n.*45+97C=
NM_031900.3:c.*142C=	NP_114106.1:n.*142C=
XM_005248337.2:c.*142C=	XP_005248394.1:n.*142C=
XM_005248338.2:c.*142C=	XP_005248395.1:n.*142C=
XM_011514077.1:c.1438-175C=	XP_011512379.1:n.1438-175C=
XM_005248337.3:c.*142C=	XP_005248394.1:n.*142C=
XM_005248338.3:c.*142C=	XP_005248395.1:n.*142C=
XM_017009748.2:c.*142C=	XP_016865237.1:n.*142C=
NM_031900.4:c.*142C= MANE Select	NP_114106.1:n.*142C=
NM_001306173.2:c.*45+97C=	NP_001293102.1:n.*45+97C=