Canonical Allele Identifier: CA1177628423

Gene: NEXN

Linked Data

• dbSNP Id: rs1557991524
• gnomAD v4: 1-77936183-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936183A>G , CM000663.2:g.77936183A>G	GRCh38
NC_000001.10:g.78401868A>G , CM000663.1:g.78401868A>G	GRCh37
NC_000001.9:g.78174456A>G	NCBI36
NG_016625.1:g.52669A>G , LRG_442:g.52669A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+139A>G MANE Select	ENSP00000333938.7:n.1473+139A>G
ENST00000330010.12:c.1281+139A>G	ENSP00000327363.8:n.1281+139A>G
ENST00000334785.11:c.1473+139A>G	ENSP00000333938.7:n.1473+139A>G
ENST00000342754.5:c.1172+139A>G
ENST00000480732.2:n.1047+139A>G
NM_001172309.1:c.1281+139A>G	NP_001165780.1:n.1281+139A>G
NM_144573.3:c.1473+139A>G , LRG_442t1:c.1473+139A>G	NP_653174.3:n.1473+139A>G
XM_005271322.2:c.1473+139A>G	XP_005271379.1:n.1473+139A>G
XM_005271323.2:c.1431+139A>G	XP_005271380.1:n.1431+139A>G
XM_005271324.3:c.1281+139A>G	XP_005271381.1:n.1281+139A>G
XM_005271325.2:c.1251+2704A>G	XP_005271382.1:n.1251+2704A>G
XM_005271326.2:c.1239+139A>G	XP_005271383.1:n.1239+139A>G
XM_005271327.2:c.1056+139A>G	XP_005271384.1:n.1056+139A>G
XM_005271322.4:c.1473+139A>G	XP_005271379.1:n.1473+139A>G
XM_005271323.4:c.1431+139A>G	XP_005271380.1:n.1431+139A>G
XM_005271324.5:c.1281+139A>G	XP_005271381.1:n.1281+139A>G
XM_005271325.4:c.1251+2704A>G	XP_005271382.1:n.1251+2704A>G
XM_005271326.4:c.1239+139A>G	XP_005271383.1:n.1239+139A>G
XM_005271327.4:c.1056+139A>G	XP_005271384.1:n.1056+139A>G
NM_001172309.2:c.1281+139A>G	NP_001165780.1:n.1281+139A>G
NM_144573.4:c.1473+139A>G MANE Select	NP_653174.3:n.1473+139A>G