Canonical Allele Identifier: CA2744232125

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935521_77935522insC , CM000663.2:g.77935521_77935522insC	GRCh38
NC_000001.10:g.78401206_78401207insC , CM000663.1:g.78401206_78401207insC	GRCh37
NC_000001.9:g.78173794_78173795insC	NCBI36
NG_016625.1:g.52007_52008insC , LRG_442:g.52007_52008insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-302_1252-301insC MANE Select	ENSP00000333938.7:n.1252-302_1252-301insC
ENST00000330010.12:c.1060-302_1060-301insC	ENSP00000327363.8:n.1060-302_1060-301insC
ENST00000334785.11:c.1252-302_1252-301insC	ENSP00000333938.7:n.1252-302_1252-301insC
ENST00000342754.5:c.951-302_951-301insC
ENST00000440324.5:c.1210-302_1210-301insC	ENSP00000411902.1:n.1210-302_1210-301insC
ENST00000464998.1:n.712-302_712-301insC
ENST00000480732.2:n.826-302_826-301insC
NM_001172309.1:c.1060-302_1060-301insC	NP_001165780.1:n.1060-302_1060-301insC
NM_144573.3:c.1252-302_1252-301insC , LRG_442t1:c.1252-302_1252-301insC	NP_653174.3:n.1252-302_1252-301insC
XM_005271322.2:c.1252-302_1252-301insC	XP_005271379.1:n.1252-302_1252-301insC
XM_005271323.2:c.1210-302_1210-301insC	XP_005271380.1:n.1210-302_1210-301insC
XM_005271324.3:c.1060-302_1060-301insC	XP_005271381.1:n.1060-302_1060-301insC
XM_005271325.2:c.1251+2042_1251+2043insC	XP_005271382.1:n.1251+2042_1251+2043insC
XM_005271326.2:c.1018-302_1018-301insC	XP_005271383.1:n.1018-302_1018-301insC
XM_005271327.2:c.835-302_835-301insC	XP_005271384.1:n.835-302_835-301insC
XM_005271322.4:c.1252-302_1252-301insC	XP_005271379.1:n.1252-302_1252-301insC
XM_005271323.4:c.1210-302_1210-301insC	XP_005271380.1:n.1210-302_1210-301insC
XM_005271324.5:c.1060-302_1060-301insC	XP_005271381.1:n.1060-302_1060-301insC
XM_005271325.4:c.1251+2042_1251+2043insC	XP_005271382.1:n.1251+2042_1251+2043insC
XM_005271326.4:c.1018-302_1018-301insC	XP_005271383.1:n.1018-302_1018-301insC
XM_005271327.4:c.835-302_835-301insC	XP_005271384.1:n.835-302_835-301insC
NM_001172309.2:c.1060-302_1060-301insC	NP_001165780.1:n.1060-302_1060-301insC
NM_144573.4:c.1252-302_1252-301insC MANE Select	NP_653174.3:n.1252-302_1252-301insC