Canonical Allele Identifier: CA1177628267

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935831_77935832delinsAG , CM000663.2:g.77935831_77935832delinsAG	GRCh38
NC_000001.10:g.78401516_78401517delinsAG , CM000663.1:g.78401516_78401517delinsAG	GRCh37
NC_000001.9:g.78174104_78174105delinsAG	NCBI36
NG_016625.1:g.52317_52318delinsAG , LRG_442:g.52317_52318delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1260_1261delinsAG MANE Select	ENSP00000333938.7:p.Glu420=
ENST00000330010.12:c.1068_1069delinsAG	ENSP00000327363.8:p.Glu356=
ENST00000334785.11:c.1260_1261delinsAG	ENSP00000333938.7:p.Glu420=
ENST00000342754.5:c.959_960delinsAG
ENST00000440324.5:c.1218_1219delinsAG	ENSP00000411902.1:p.Glu406=
ENST00000464998.1:n.720_721delinsAG
ENST00000480732.2:n.834_835delinsAG
NM_001172309.1:c.1068_1069delinsAG	NP_001165780.1:p.Glu356=
NM_144573.3:c.1260_1261delinsAG , LRG_442t1:c.1260_1261delinsAG	NP_653174.3:p.Glu420=
XM_005271322.2:c.1260_1261delinsAG	XP_005271379.1:p.Glu420=
XM_005271323.2:c.1218_1219delinsAG	XP_005271380.1:p.Glu406=
XM_005271324.3:c.1068_1069delinsAG	XP_005271381.1:p.Glu356=
XM_005271325.2:c.1251+2352_1251+2353delinsAG	XP_005271382.1:n.1251+2352_1251+2353delinsAG
XM_005271326.2:c.1026_1027delinsAG	XP_005271383.1:p.Glu342=
XM_005271327.2:c.843_844delinsAG	XP_005271384.1:p.Glu281=
XM_005271322.4:c.1260_1261delinsAG	XP_005271379.1:p.Glu420=
XM_005271323.4:c.1218_1219delinsAG	XP_005271380.1:p.Glu406=
XM_005271324.5:c.1068_1069delinsAG	XP_005271381.1:p.Glu356=
XM_005271325.4:c.1251+2352_1251+2353delinsAG	XP_005271382.1:n.1251+2352_1251+2353delinsAG
XM_005271326.4:c.1026_1027delinsAG	XP_005271383.1:p.Glu342=
XM_005271327.4:c.843_844delinsAG	XP_005271384.1:p.Glu281=
NM_001172309.2:c.1068_1069delinsAG	NP_001165780.1:p.Glu356=
NM_144573.4:c.1260_1261delinsAG MANE Select	NP_653174.3:p.Glu420=