Canonical Allele Identifier: CA2600639597

Gene: NEXN

Linked Data

• dbSNP Id: rs2102147542
• gnomAD v3: 1-77933572-C-G
• gnomAD v4: 1-77933572-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933572C>G , CM000663.2:g.77933572C>G	GRCh38
NC_000001.10:g.78399257C>G , CM000663.1:g.78399257C>G	GRCh37
NC_000001.9:g.78171845C>G	NCBI36
NG_016625.1:g.50058C>G , LRG_442:g.50058C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+93C>G MANE Select	ENSP00000333938.7:n.1251+93C>G
ENST00000330010.12:c.1059+93C>G	ENSP00000327363.8:n.1059+93C>G
ENST00000334785.11:c.1251+93C>G	ENSP00000333938.7:n.1251+93C>G
ENST00000342754.5:c.950+93C>G
ENST00000440324.5:c.1209+93C>G	ENSP00000411902.1:n.1209+93C>G
ENST00000464998.1:n.711+93C>G
ENST00000480732.2:n.825+93C>G
NM_001172309.1:c.1059+93C>G	NP_001165780.1:n.1059+93C>G
NM_144573.3:c.1251+93C>G , LRG_442t1:c.1251+93C>G	NP_653174.3:n.1251+93C>G
XM_005271322.2:c.1251+93C>G	XP_005271379.1:n.1251+93C>G
XM_005271323.2:c.1209+93C>G	XP_005271380.1:n.1209+93C>G
XM_005271324.3:c.1059+93C>G	XP_005271381.1:n.1059+93C>G
XM_005271325.2:c.1251+93C>G	XP_005271382.1:n.1251+93C>G
XM_005271326.2:c.1017+93C>G	XP_005271383.1:n.1017+93C>G
XM_005271327.2:c.834+93C>G	XP_005271384.1:n.834+93C>G
XM_005271322.4:c.1251+93C>G	XP_005271379.1:n.1251+93C>G
XM_005271323.4:c.1209+93C>G	XP_005271380.1:n.1209+93C>G
XM_005271324.5:c.1059+93C>G	XP_005271381.1:n.1059+93C>G
XM_005271325.4:c.1251+93C>G	XP_005271382.1:n.1251+93C>G
XM_005271326.4:c.1017+93C>G	XP_005271383.1:n.1017+93C>G
XM_005271327.4:c.834+93C>G	XP_005271384.1:n.834+93C>G
NM_001172309.2:c.1059+93C>G	NP_001165780.1:n.1059+93C>G
NM_144573.4:c.1251+93C>G MANE Select	NP_653174.3:n.1251+93C>G