Canonical Allele Identifier: CA340881505

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407862A>G (hg19) ; chr1:g.77942177A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942177A>G , CM000663.2:g.77942177A>G	GRCh38
NC_000001.10:g.78407862A>G , CM000663.1:g.78407862A>G	GRCh37
NC_000001.9:g.78180450A>G	NCBI36
NG_016625.1:g.58663A>G , LRG_442:g.58663A>G
NG_033243.2:g.41917T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1628A>G MANE Select	ENSP00000333938.7:p.Glu543Gly
ENST00000330010.12:c.1436A>G	ENSP00000327363.8:p.Glu479Gly
ENST00000334785.11:c.1628A>G	ENSP00000333938.7:p.Glu543Gly
ENST00000342754.5:c.1327A>G
ENST00000470735.1:n.467A>G
ENST00000480732.2:n.1202A>G
NM_001172309.1:c.1436A>G	NP_001165780.1:p.Glu479Gly
NM_144573.3:c.1628A>G , LRG_442t1:c.1628A>G	NP_653174.3:p.Glu543Gly
XM_005271322.2:c.1628A>G	XP_005271379.1:p.Glu543Gly
XM_005271323.2:c.1586A>G	XP_005271380.1:p.Glu529Gly
XM_005271324.3:c.1436A>G	XP_005271381.1:p.Glu479Gly
XM_005271325.2:c.1406A>G	XP_005271382.1:p.Glu469Gly
XM_005271326.2:c.1394A>G	XP_005271383.1:p.Glu465Gly
XM_005271327.2:c.1211A>G	XP_005271384.1:p.Glu404Gly
XM_005271322.4:c.1628A>G	XP_005271379.1:p.Glu543Gly
XM_005271323.4:c.1586A>G	XP_005271380.1:p.Glu529Gly
XM_005271324.5:c.1436A>G	XP_005271381.1:p.Glu479Gly
XM_005271325.4:c.1406A>G	XP_005271382.1:p.Glu469Gly
XM_005271326.4:c.1394A>G	XP_005271383.1:p.Glu465Gly
XM_005271327.4:c.1211A>G	XP_005271384.1:p.Glu404Gly
NM_001172309.2:c.1436A>G	NP_001165780.1:p.Glu479Gly
NM_144573.4:c.1628A>G MANE Select	NP_653174.3:p.Glu543Gly