Canonical Allele Identifier: CA1177628154

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935598_77935601delinsTAAG , CM000663.2:g.77935598_77935601delinsTAAG	GRCh38
NC_000001.10:g.78401283_78401286delinsTAAG , CM000663.1:g.78401283_78401286delinsTAAG	GRCh37
NC_000001.9:g.78173871_78173874delinsTAAG	NCBI36
NG_016625.1:g.52084_52087delinsTAAG , LRG_442:g.52084_52087delinsTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-225_1252-222delinsTAAG MANE Select	ENSP00000333938.7:n.1252-225_1252-222delinsTAAG
ENST00000330010.12:c.1060-225_1060-222delinsTAAG	ENSP00000327363.8:n.1060-225_1060-222delinsTAAG
ENST00000334785.11:c.1252-225_1252-222delinsTAAG	ENSP00000333938.7:n.1252-225_1252-222delinsTAAG
ENST00000342754.5:c.951-225_951-222delinsTAAG
ENST00000440324.5:c.1210-225_1210-222delinsTAAG	ENSP00000411902.1:n.1210-225_1210-222delinsTAAG
ENST00000464998.1:n.712-225_712-222delinsTAAG
ENST00000480732.2:n.826-225_826-222delinsTAAG
NM_001172309.1:c.1060-225_1060-222delinsTAAG	NP_001165780.1:n.1060-225_1060-222delinsTAAG
NM_144573.3:c.1252-225_1252-222delinsTAAG , LRG_442t1:c.1252-225_1252-222delinsTAAG	NP_653174.3:n.1252-225_1252-222delinsTAAG
XM_005271322.2:c.1252-225_1252-222delinsTAAG	XP_005271379.1:n.1252-225_1252-222delinsTAAG
XM_005271323.2:c.1210-225_1210-222delinsTAAG	XP_005271380.1:n.1210-225_1210-222delinsTAAG
XM_005271324.3:c.1060-225_1060-222delinsTAAG	XP_005271381.1:n.1060-225_1060-222delinsTAAG
XM_005271325.2:c.1251+2119_1251+2122delinsTAAG	XP_005271382.1:n.1251+2119_1251+2122delinsTAAG
XM_005271326.2:c.1018-225_1018-222delinsTAAG	XP_005271383.1:n.1018-225_1018-222delinsTAAG
XM_005271327.2:c.835-225_835-222delinsTAAG	XP_005271384.1:n.835-225_835-222delinsTAAG
XM_005271322.4:c.1252-225_1252-222delinsTAAG	XP_005271379.1:n.1252-225_1252-222delinsTAAG
XM_005271323.4:c.1210-225_1210-222delinsTAAG	XP_005271380.1:n.1210-225_1210-222delinsTAAG
XM_005271324.5:c.1060-225_1060-222delinsTAAG	XP_005271381.1:n.1060-225_1060-222delinsTAAG
XM_005271325.4:c.1251+2119_1251+2122delinsTAAG	XP_005271382.1:n.1251+2119_1251+2122delinsTAAG
XM_005271326.4:c.1018-225_1018-222delinsTAAG	XP_005271383.1:n.1018-225_1018-222delinsTAAG
XM_005271327.4:c.835-225_835-222delinsTAAG	XP_005271384.1:n.835-225_835-222delinsTAAG
NM_001172309.2:c.1060-225_1060-222delinsTAAG	NP_001165780.1:n.1060-225_1060-222delinsTAAG
NM_144573.4:c.1252-225_1252-222delinsTAAG MANE Select	NP_653174.3:n.1252-225_1252-222delinsTAAG