Canonical Allele Identifier: CA340883148

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408386G>C (hg19) ; chr1:g.77942701G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942701G>C , CM000663.2:g.77942701G>C	GRCh38
NC_000001.10:g.78408386G>C , CM000663.1:g.78408386G>C	GRCh37
NC_000001.9:g.78180974G>C	NCBI36
NG_016625.1:g.59187G>C , LRG_442:g.59187G>C
NG_033243.2:g.41393C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1900G>C MANE Select	ENSP00000333938.7:p.Gly634Arg
ENST00000330010.12:c.1708G>C	ENSP00000327363.8:p.Gly570Arg
ENST00000334785.11:c.1900G>C	ENSP00000333938.7:p.Gly634Arg
ENST00000342754.5:c.1599G>C
ENST00000470735.1:n.739G>C
ENST00000480732.2:n.1474G>C
NM_001172309.1:c.1708G>C	NP_001165780.1:p.Gly570Arg
NM_144573.3:c.1900G>C , LRG_442t1:c.1900G>C	NP_653174.3:p.Gly634Arg
XM_005271322.2:c.1900G>C	XP_005271379.1:p.Gly634Arg
XM_005271323.2:c.1858G>C	XP_005271380.1:p.Gly620Arg
XM_005271324.3:c.1708G>C	XP_005271381.1:p.Gly570Arg
XM_005271325.2:c.1678G>C	XP_005271382.1:p.Gly560Arg
XM_005271326.2:c.1666G>C	XP_005271383.1:p.Gly556Arg
XM_005271327.2:c.1483G>C	XP_005271384.1:p.Gly495Arg
XM_005271322.4:c.1900G>C	XP_005271379.1:p.Gly634Arg
XM_005271323.4:c.1858G>C	XP_005271380.1:p.Gly620Arg
XM_005271324.5:c.1708G>C	XP_005271381.1:p.Gly570Arg
XM_005271325.4:c.1678G>C	XP_005271382.1:p.Gly560Arg
XM_005271326.4:c.1666G>C	XP_005271383.1:p.Gly556Arg
XM_005271327.4:c.1483G>C	XP_005271384.1:p.Gly495Arg
NM_001172309.2:c.1708G>C	NP_001165780.1:p.Gly570Arg
NM_144573.4:c.1900G>C MANE Select	NP_653174.3:p.Gly634Arg