Canonical Allele Identifier: CA1177628206

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935723_77935726delinsCAGG , CM000663.2:g.77935723_77935726delinsCAGG	GRCh38
NC_000001.10:g.78401408_78401411delinsCAGG , CM000663.1:g.78401408_78401411delinsCAGG	GRCh37
NC_000001.9:g.78173996_78173999delinsCAGG	NCBI36
NG_016625.1:g.52209_52212delinsCAGG , LRG_442:g.52209_52212delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-100_1252-97delinsCAGG MANE Select	ENSP00000333938.7:n.1252-100_1252-97delinsCAGG
ENST00000330010.12:c.1060-100_1060-97delinsCAGG	ENSP00000327363.8:n.1060-100_1060-97delinsCAGG
ENST00000334785.11:c.1252-100_1252-97delinsCAGG	ENSP00000333938.7:n.1252-100_1252-97delinsCAGG
ENST00000342754.5:c.951-100_951-97delinsCAGG
ENST00000440324.5:c.1210-100_1210-97delinsCAGG	ENSP00000411902.1:n.1210-100_1210-97delinsCAGG
ENST00000464998.1:n.712-100_712-97delinsCAGG
ENST00000480732.2:n.826-100_826-97delinsCAGG
NM_001172309.1:c.1060-100_1060-97delinsCAGG	NP_001165780.1:n.1060-100_1060-97delinsCAGG
NM_144573.3:c.1252-100_1252-97delinsCAGG , LRG_442t1:c.1252-100_1252-97delinsCAGG	NP_653174.3:n.1252-100_1252-97delinsCAGG
XM_005271322.2:c.1252-100_1252-97delinsCAGG	XP_005271379.1:n.1252-100_1252-97delinsCAGG
XM_005271323.2:c.1210-100_1210-97delinsCAGG	XP_005271380.1:n.1210-100_1210-97delinsCAGG
XM_005271324.3:c.1060-100_1060-97delinsCAGG	XP_005271381.1:n.1060-100_1060-97delinsCAGG
XM_005271325.2:c.1251+2244_1251+2247delinsCAGG	XP_005271382.1:n.1251+2244_1251+2247delinsCAGG
XM_005271326.2:c.1018-100_1018-97delinsCAGG	XP_005271383.1:n.1018-100_1018-97delinsCAGG
XM_005271327.2:c.835-100_835-97delinsCAGG	XP_005271384.1:n.835-100_835-97delinsCAGG
XM_005271322.4:c.1252-100_1252-97delinsCAGG	XP_005271379.1:n.1252-100_1252-97delinsCAGG
XM_005271323.4:c.1210-100_1210-97delinsCAGG	XP_005271380.1:n.1210-100_1210-97delinsCAGG
XM_005271324.5:c.1060-100_1060-97delinsCAGG	XP_005271381.1:n.1060-100_1060-97delinsCAGG
XM_005271325.4:c.1251+2244_1251+2247delinsCAGG	XP_005271382.1:n.1251+2244_1251+2247delinsCAGG
XM_005271326.4:c.1018-100_1018-97delinsCAGG	XP_005271383.1:n.1018-100_1018-97delinsCAGG
XM_005271327.4:c.835-100_835-97delinsCAGG	XP_005271384.1:n.835-100_835-97delinsCAGG
NM_001172309.2:c.1060-100_1060-97delinsCAGG	NP_001165780.1:n.1060-100_1060-97delinsCAGG
NM_144573.4:c.1252-100_1252-97delinsCAGG MANE Select	NP_653174.3:n.1252-100_1252-97delinsCAGG