Canonical Allele Identifier: CA918865
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs767709993
gnomAD v2: 1-78401631-T-C
gnomAD v4: 1-77935946-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935946T>C , CM000663.2:g.77935946T>C GRCh38
NC_000001.10:g.78401631T>C , CM000663.1:g.78401631T>C GRCh37
NC_000001.9:g.78174219T>C NCBI36
NG_016625.1:g.52432T>C , LRG_442:g.52432T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1375T>C MANE Select ENSP00000333938.7:p.Ser459Pro
ENST00000330010.12:c.1183T>C ENSP00000327363.8:p.Ser395Pro
ENST00000334785.11:c.1375T>C ENSP00000333938.7:p.Ser459Pro
ENST00000342754.5:c.1074T>C
ENST00000464998.1:n.835T>C
ENST00000480732.2:n.949T>C
NM_001172309.1:c.1183T>C NP_001165780.1:p.Ser395Pro
NM_144573.3:c.1375T>C , LRG_442t1:c.1375T>C NP_653174.3:p.Ser459Pro
XM_005271322.2:c.1375T>C XP_005271379.1:p.Ser459Pro
XM_005271323.2:c.1333T>C XP_005271380.1:p.Ser445Pro
XM_005271324.3:c.1183T>C XP_005271381.1:p.Ser395Pro
XM_005271325.2:c.1251+2467T>C XP_005271382.1:n.1251+2467T>C
XM_005271326.2:c.1141T>C XP_005271383.1:p.Ser381Pro
XM_005271327.2:c.958T>C XP_005271384.1:p.Ser320Pro
XM_005271322.4:c.1375T>C XP_005271379.1:p.Ser459Pro
XM_005271323.4:c.1333T>C XP_005271380.1:p.Ser445Pro
XM_005271324.5:c.1183T>C XP_005271381.1:p.Ser395Pro
XM_005271325.4:c.1251+2467T>C XP_005271382.1:n.1251+2467T>C
XM_005271326.4:c.1141T>C XP_005271383.1:p.Ser381Pro
XM_005271327.4:c.958T>C XP_005271384.1:p.Ser320Pro
NM_001172309.2:c.1183T>C NP_001165780.1:p.Ser395Pro
NM_144573.4:c.1375T>C MANE Select NP_653174.3:p.Ser459Pro