Canonical Allele Identifier: CA645565428

Gene: AGXT2

Linked Data

• COSMIC: COSM4614025

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998768_34998770del , CM000667.2:g.34998768_34998770del	GRCh38
NC_000005.9:g.34998873_34998875del , CM000667.1:g.34998873_34998875del	GRCh37
NC_000005.8:g.35034630_35034632del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1496_1498del MANE Select	ENSP00000231420.6:p.Glu499del
ENST00000231420.10:c.1496_1498del	ENSP00000231420.6:p.Glu499del
ENST00000510428.1:c.1271_1273del	ENSP00000422799.1:p.Glu424del
ENST00000512135.5:n.1166_1168del
ENST00000618015.4:c.1271_1273del	ENSP00000479154.1:p.Glu424del
NM_001306173.1:c.1271_1273del	NP_001293102.1:p.Glu424del
NM_031900.3:c.1496_1498del	NP_114106.1:p.Glu499del
XM_005248337.2:c.1493_1495del	XP_005248394.1:p.Glu498del
XM_005248338.2:c.1301_1303del	XP_005248395.1:p.Glu434del
XM_011514077.1:c.1438-366_1438-364del	XP_011512379.1:n.1438-366_1438-364del
XM_005248337.3:c.1493_1495del	XP_005248394.1:p.Glu498del
XM_005248338.3:c.1301_1303del	XP_005248395.1:p.Glu434del
XM_017009748.2:c.1271_1273del	XP_016865237.1:p.Glu424del
NM_031900.4:c.1496_1498del MANE Select	NP_114106.1:p.Glu499del
NM_001306173.2:c.1271_1273del	NP_001293102.1:p.Glu424del