Canonical Allele Identifier: CA1538676627

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998742G= , CM000667.2:g.34998742G=	GRCh38
NC_000005.9:g.34998847G= , CM000667.1:g.34998847G=	GRCh37
NC_000005.8:g.35034604G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1522C= MANE Select	ENSP00000231420.6:p.His508=
ENST00000231420.10:c.1522C=	ENSP00000231420.6:p.His508=
ENST00000510428.1:c.1297C=	ENSP00000422799.1:p.His433=
ENST00000512135.5:n.1192C=
ENST00000618015.4:c.1297C=	ENSP00000479154.1:p.His433=
NM_001306173.1:c.1297C=	NP_001293102.1:p.His433=
NM_031900.3:c.1522C=	NP_114106.1:p.His508=
XM_005248337.2:c.1519C=	XP_005248394.1:p.His507=
XM_005248338.2:c.1327C=	XP_005248395.1:p.His443=
XM_011514077.1:c.1438-340C=	XP_011512379.1:n.1438-340C=
XM_005248337.3:c.1519C=	XP_005248394.1:p.His507=
XM_005248338.3:c.1327C=	XP_005248395.1:p.His443=
XM_017009748.2:c.1297C=	XP_016865237.1:p.His433=
NM_031900.4:c.1522C= MANE Select	NP_114106.1:p.His508=
NM_001306173.2:c.1297C=	NP_001293102.1:p.His433=