Canonical Allele Identifier: CA1538676806

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998814_34998815delinsCA , CM000667.2:g.34998814_34998815delinsCA	GRCh38
NC_000005.9:g.34998919_34998920delinsCA , CM000667.1:g.34998919_34998920delinsCA	GRCh37
NC_000005.8:g.35034676_35034677delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1449_1450delinsTG MANE Select	ENSP00000231420.6:p.Ile483=
ENST00000231420.10:c.1449_1450delinsTG	ENSP00000231420.6:p.Ile483=
ENST00000510428.1:c.1224_1225delinsTG	ENSP00000422799.1:p.Ile408=
ENST00000512135.5:n.1119_1120delinsTG
ENST00000618015.4:c.1224_1225delinsTG	ENSP00000479154.1:p.Ile408=
NM_001306173.1:c.1224_1225delinsTG	NP_001293102.1:p.Ile408=
NM_031900.3:c.1449_1450delinsTG	NP_114106.1:p.Ile483=
XM_005248337.2:c.1446_1447delinsTG	XP_005248394.1:p.Ile482=
XM_005248338.2:c.1254_1255delinsTG	XP_005248395.1:p.Ile418=
XM_011514077.1:c.1438-413_1438-412delinsTG	XP_011512379.1:n.1438-413_1438-412delinsTG
XM_005248337.3:c.1446_1447delinsTG	XP_005248394.1:p.Ile482=
XM_005248338.3:c.1254_1255delinsTG	XP_005248395.1:p.Ile418=
XM_017009748.2:c.1224_1225delinsTG	XP_016865237.1:p.Ile408=
NM_031900.4:c.1449_1450delinsTG MANE Select	NP_114106.1:p.Ile483=
NM_001306173.2:c.1224_1225delinsTG	NP_001293102.1:p.Ile408=