Canonical Allele Identifier: CA340878298

Gene: NEXN

Linked Data

• gnomAD v4: 1-77935855-C-G
• MyVariant Identifiers: chr1:g.78401540C>G (hg19) ; chr1:g.77935855C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935855C>G , CM000663.2:g.77935855C>G	GRCh38
NC_000001.10:g.78401540C>G , CM000663.1:g.78401540C>G	GRCh37
NC_000001.9:g.78174128C>G	NCBI36
NG_016625.1:g.52341C>G , LRG_442:g.52341C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1284C>G MANE Select	ENSP00000333938.7:p.Ser428Arg
ENST00000330010.12:c.1092C>G	ENSP00000327363.8:p.Ser364Arg
ENST00000334785.11:c.1284C>G	ENSP00000333938.7:p.Ser428Arg
ENST00000342754.5:c.983C>G
ENST00000440324.5:c.1242C>G	ENSP00000411902.1:p.Ser414Arg
ENST00000464998.1:n.744C>G
ENST00000480732.2:n.858C>G
NM_001172309.1:c.1092C>G	NP_001165780.1:p.Ser364Arg
NM_144573.3:c.1284C>G , LRG_442t1:c.1284C>G	NP_653174.3:p.Ser428Arg
XM_005271322.2:c.1284C>G	XP_005271379.1:p.Ser428Arg
XM_005271323.2:c.1242C>G	XP_005271380.1:p.Ser414Arg
XM_005271324.3:c.1092C>G	XP_005271381.1:p.Ser364Arg
XM_005271325.2:c.1251+2376C>G	XP_005271382.1:n.1251+2376C>G
XM_005271326.2:c.1050C>G	XP_005271383.1:p.Ser350Arg
XM_005271327.2:c.867C>G	XP_005271384.1:p.Ser289Arg
XM_005271322.4:c.1284C>G	XP_005271379.1:p.Ser428Arg
XM_005271323.4:c.1242C>G	XP_005271380.1:p.Ser414Arg
XM_005271324.5:c.1092C>G	XP_005271381.1:p.Ser364Arg
XM_005271325.4:c.1251+2376C>G	XP_005271382.1:n.1251+2376C>G
XM_005271326.4:c.1050C>G	XP_005271383.1:p.Ser350Arg
XM_005271327.4:c.867C>G	XP_005271384.1:p.Ser289Arg
NM_001172309.2:c.1092C>G	NP_001165780.1:p.Ser364Arg
NM_144573.4:c.1284C>G MANE Select	NP_653174.3:p.Ser428Arg