Canonical Allele Identifier: CA1177628176

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935669_77935671delinsTGA , CM000663.2:g.77935669_77935671delinsTGA	GRCh38
NC_000001.10:g.78401354_78401356delinsTGA , CM000663.1:g.78401354_78401356delinsTGA	GRCh37
NC_000001.9:g.78173942_78173944delinsTGA	NCBI36
NG_016625.1:g.52155_52157delinsTGA , LRG_442:g.52155_52157delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-154_1252-152delinsTGA MANE Select	ENSP00000333938.7:n.1252-154_1252-152delinsTGA
ENST00000330010.12:c.1060-154_1060-152delinsTGA	ENSP00000327363.8:n.1060-154_1060-152delinsTGA
ENST00000334785.11:c.1252-154_1252-152delinsTGA	ENSP00000333938.7:n.1252-154_1252-152delinsTGA
ENST00000342754.5:c.951-154_951-152delinsTGA
ENST00000440324.5:c.1210-154_1210-152delinsTGA	ENSP00000411902.1:n.1210-154_1210-152delinsTGA
ENST00000464998.1:n.712-154_712-152delinsTGA
ENST00000480732.2:n.826-154_826-152delinsTGA
NM_001172309.1:c.1060-154_1060-152delinsTGA	NP_001165780.1:n.1060-154_1060-152delinsTGA
NM_144573.3:c.1252-154_1252-152delinsTGA , LRG_442t1:c.1252-154_1252-152delinsTGA	NP_653174.3:n.1252-154_1252-152delinsTGA
XM_005271322.2:c.1252-154_1252-152delinsTGA	XP_005271379.1:n.1252-154_1252-152delinsTGA
XM_005271323.2:c.1210-154_1210-152delinsTGA	XP_005271380.1:n.1210-154_1210-152delinsTGA
XM_005271324.3:c.1060-154_1060-152delinsTGA	XP_005271381.1:n.1060-154_1060-152delinsTGA
XM_005271325.2:c.1251+2190_1251+2192delinsTGA	XP_005271382.1:n.1251+2190_1251+2192delinsTGA
XM_005271326.2:c.1018-154_1018-152delinsTGA	XP_005271383.1:n.1018-154_1018-152delinsTGA
XM_005271327.2:c.835-154_835-152delinsTGA	XP_005271384.1:n.835-154_835-152delinsTGA
XM_005271322.4:c.1252-154_1252-152delinsTGA	XP_005271379.1:n.1252-154_1252-152delinsTGA
XM_005271323.4:c.1210-154_1210-152delinsTGA	XP_005271380.1:n.1210-154_1210-152delinsTGA
XM_005271324.5:c.1060-154_1060-152delinsTGA	XP_005271381.1:n.1060-154_1060-152delinsTGA
XM_005271325.4:c.1251+2190_1251+2192delinsTGA	XP_005271382.1:n.1251+2190_1251+2192delinsTGA
XM_005271326.4:c.1018-154_1018-152delinsTGA	XP_005271383.1:n.1018-154_1018-152delinsTGA
XM_005271327.4:c.835-154_835-152delinsTGA	XP_005271384.1:n.835-154_835-152delinsTGA
NM_001172309.2:c.1060-154_1060-152delinsTGA	NP_001165780.1:n.1060-154_1060-152delinsTGA
NM_144573.4:c.1252-154_1252-152delinsTGA MANE Select	NP_653174.3:n.1252-154_1252-152delinsTGA