Canonical Allele Identifier: CA524231064

Gene: NEXN

Linked Data

• dbSNP Id: rs1256799625
• gnomAD v2: 1-78407662-T-G
• gnomAD v4: 1-77941977-T-G
• MyVariant Identifiers: chr1:g.78407662T>G (hg19) ; chr1:g.77941977T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77941977T>G , CM000663.2:g.77941977T>G	GRCh38
NC_000001.10:g.78407662T>G , CM000663.1:g.78407662T>G	GRCh37
NC_000001.9:g.78180250T>G	NCBI36
NG_016625.1:g.58463T>G , LRG_442:g.58463T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1474-46T>G MANE Select	ENSP00000333938.7:n.1474-46T>G
ENST00000330010.12:c.1282-46T>G	ENSP00000327363.8:n.1282-46T>G
ENST00000334785.11:c.1474-46T>G	ENSP00000333938.7:n.1474-46T>G
ENST00000342754.5:c.1173-46T>G
ENST00000470735.1:n.267T>G
ENST00000480732.2:n.1048-46T>G
NM_001172309.1:c.1282-46T>G	NP_001165780.1:n.1282-46T>G
NM_144573.3:c.1474-46T>G , LRG_442t1:c.1474-46T>G	NP_653174.3:n.1474-46T>G
XM_005271322.2:c.1474-46T>G	XP_005271379.1:n.1474-46T>G
XM_005271323.2:c.1432-46T>G	XP_005271380.1:n.1432-46T>G
XM_005271324.3:c.1282-46T>G	XP_005271381.1:n.1282-46T>G
XM_005271325.2:c.1252-46T>G	XP_005271382.1:n.1252-46T>G
XM_005271326.2:c.1240-46T>G	XP_005271383.1:n.1240-46T>G
XM_005271327.2:c.1057-46T>G	XP_005271384.1:n.1057-46T>G
XM_005271322.4:c.1474-46T>G	XP_005271379.1:n.1474-46T>G
XM_005271323.4:c.1432-46T>G	XP_005271380.1:n.1432-46T>G
XM_005271324.5:c.1282-46T>G	XP_005271381.1:n.1282-46T>G
XM_005271325.4:c.1252-46T>G	XP_005271382.1:n.1252-46T>G
XM_005271326.4:c.1240-46T>G	XP_005271383.1:n.1240-46T>G
XM_005271327.4:c.1057-46T>G	XP_005271384.1:n.1057-46T>G
NM_001172309.2:c.1282-46T>G	NP_001165780.1:n.1282-46T>G
NM_144573.4:c.1474-46T>G MANE Select	NP_653174.3:n.1474-46T>G