Canonical Allele Identifier: CA1538676863

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998846_34998849delinsTAAG , CM000667.2:g.34998846_34998849delinsTAAG	GRCh38
NC_000005.9:g.34998951_34998954delinsTAAG , CM000667.1:g.34998951_34998954delinsTAAG	GRCh37
NC_000005.8:g.35034708_35034711delinsTAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1438-23_1438-20delinsCTTA MANE Select	ENSP00000231420.6:n.1438-23_1438-20delinsCTTA
ENST00000231420.10:c.1438-23_1438-20delinsCTTA	ENSP00000231420.6:n.1438-23_1438-20delinsCTTA
ENST00000510428.1:c.1213-23_1213-20delinsCTTA	ENSP00000422799.1:n.1213-23_1213-20delinsCTTA
ENST00000512135.5:n.1108-23_1108-20delinsCTTA
ENST00000618015.4:c.1213-23_1213-20delinsCTTA	ENSP00000479154.1:n.1213-23_1213-20delinsCTTA
NM_001306173.1:c.1213-23_1213-20delinsCTTA	NP_001293102.1:n.1213-23_1213-20delinsCTTA
NM_031900.3:c.1438-23_1438-20delinsCTTA	NP_114106.1:n.1438-23_1438-20delinsCTTA
XM_005248337.2:c.1435-23_1435-20delinsCTTA	XP_005248394.1:n.1435-23_1435-20delinsCTTA
XM_005248338.2:c.1243-23_1243-20delinsCTTA	XP_005248395.1:n.1243-23_1243-20delinsCTTA
XM_011514077.1:c.1438-447_1438-444delinsCTTA	XP_011512379.1:n.1438-447_1438-444delinsCTTA
XM_005248337.3:c.1435-23_1435-20delinsCTTA	XP_005248394.1:n.1435-23_1435-20delinsCTTA
XM_005248338.3:c.1243-23_1243-20delinsCTTA	XP_005248395.1:n.1243-23_1243-20delinsCTTA
XM_017009748.2:c.1213-23_1213-20delinsCTTA	XP_016865237.1:n.1213-23_1213-20delinsCTTA
NM_031900.4:c.1438-23_1438-20delinsCTTA MANE Select	NP_114106.1:n.1438-23_1438-20delinsCTTA
NM_001306173.2:c.1213-23_1213-20delinsCTTA	NP_001293102.1:n.1213-23_1213-20delinsCTTA