Canonical Allele Identifier: CA1538676738

Gene: AGXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998787_34998788delinsCT , CM000667.2:g.34998787_34998788delinsCT	GRCh38
NC_000005.9:g.34998892_34998893delinsCT , CM000667.1:g.34998892_34998893delinsCT	GRCh37
NC_000005.8:g.35034649_35034650delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.1476_1477delinsAG MANE Select	ENSP00000231420.6:p.Pro492=
ENST00000231420.10:c.1476_1477delinsAG	ENSP00000231420.6:p.Pro492=
ENST00000510428.1:c.1251_1252delinsAG	ENSP00000422799.1:p.Pro417=
ENST00000512135.5:n.1146_1147delinsAG
ENST00000618015.4:c.1251_1252delinsAG	ENSP00000479154.1:p.Pro417=
NM_001306173.1:c.1251_1252delinsAG	NP_001293102.1:p.Pro417=
NM_031900.3:c.1476_1477delinsAG	NP_114106.1:p.Pro492=
XM_005248337.2:c.1473_1474delinsAG	XP_005248394.1:p.Pro491=
XM_005248338.2:c.1281_1282delinsAG	XP_005248395.1:p.Pro427=
XM_011514077.1:c.1438-386_1438-385delinsAG	XP_011512379.1:n.1438-386_1438-385delinsAG
XM_005248337.3:c.1473_1474delinsAG	XP_005248394.1:p.Pro491=
XM_005248338.3:c.1281_1282delinsAG	XP_005248395.1:p.Pro427=
XM_017009748.2:c.1251_1252delinsAG	XP_016865237.1:p.Pro417=
NM_031900.4:c.1476_1477delinsAG MANE Select	NP_114106.1:p.Pro492=
NM_001306173.2:c.1251_1252delinsAG	NP_001293102.1:p.Pro417=