Canonical Allele Identifier: CA1074968886

Gene: AGXT2

Linked Data

• dbSNP Id: rs1766127416
• gnomAD v3: 5-34998914-C-CACA
• gnomAD v4: 5-34998914-C-CACA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998914_34998915insACA , CM000667.2:g.34998914_34998915insACA	GRCh38
NC_000005.9:g.34999019_34999020insACA , CM000667.1:g.34999019_34999020insACA	GRCh37
NC_000005.8:g.35034776_35034777insACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1438-89_1438-88insTGT MANE Select	ENSP00000231420.6:n.1438-89_1438-88insTGT
ENST00000231420.10:c.1438-89_1438-88insTGT	ENSP00000231420.6:n.1438-89_1438-88insTGT
ENST00000510428.1:c.1213-89_1213-88insTGT	ENSP00000422799.1:n.1213-89_1213-88insTGT
ENST00000512135.5:n.1108-89_1108-88insTGT
ENST00000618015.4:c.1213-89_1213-88insTGT	ENSP00000479154.1:n.1213-89_1213-88insTGT
NM_001306173.1:c.1213-89_1213-88insTGT	NP_001293102.1:n.1213-89_1213-88insTGT
NM_031900.3:c.1438-89_1438-88insTGT	NP_114106.1:n.1438-89_1438-88insTGT
XM_005248337.2:c.1435-89_1435-88insTGT	XP_005248394.1:n.1435-89_1435-88insTGT
XM_005248338.2:c.1243-89_1243-88insTGT	XP_005248395.1:n.1243-89_1243-88insTGT
XM_011514077.1:c.1438-513_1438-512insTGT	XP_011512379.1:n.1438-513_1438-512insTGT
XM_005248337.3:c.1435-89_1435-88insTGT	XP_005248394.1:n.1435-89_1435-88insTGT
XM_005248338.3:c.1243-89_1243-88insTGT	XP_005248395.1:n.1243-89_1243-88insTGT
XM_017009748.2:c.1213-89_1213-88insTGT	XP_016865237.1:n.1213-89_1213-88insTGT
NM_031900.4:c.1438-89_1438-88insTGT MANE Select	NP_114106.1:n.1438-89_1438-88insTGT
NM_001306173.2:c.1213-89_1213-88insTGT	NP_001293102.1:n.1213-89_1213-88insTGT