Canonical Allele Identifier: CA418573334

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407815A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942130A>G , CM000663.2:g.77942130A>G	GRCh38
NC_000001.10:g.78407815A>G , CM000663.1:g.78407815A>G	GRCh37
NC_000001.9:g.78180403A>G	NCBI36
NG_016625.1:g.58616A>G , LRG_442:g.58616A>G
NG_033243.2:g.41964T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1581A>G MANE Select	ENSP00000333938.7:p.Glu527=
ENST00000330010.12:c.1389A>G	ENSP00000327363.8:p.Glu463=
ENST00000334785.11:c.1581A>G	ENSP00000333938.7:p.Glu527=
ENST00000342754.5:c.1280A>G
ENST00000470735.1:n.420A>G
ENST00000480732.2:n.1155A>G
NM_001172309.1:c.1389A>G	NP_001165780.1:p.Glu463=
NM_144573.3:c.1581A>G , LRG_442t1:c.1581A>G	NP_653174.3:p.Glu527=
XM_005271322.2:c.1581A>G	XP_005271379.1:p.Glu527=
XM_005271323.2:c.1539A>G	XP_005271380.1:p.Glu513=
XM_005271324.3:c.1389A>G	XP_005271381.1:p.Glu463=
XM_005271325.2:c.1359A>G	XP_005271382.1:p.Glu453=
XM_005271326.2:c.1347A>G	XP_005271383.1:p.Glu449=
XM_005271327.2:c.1164A>G	XP_005271384.1:p.Glu388=
XM_005271322.4:c.1581A>G	XP_005271379.1:p.Glu527=
XM_005271323.4:c.1539A>G	XP_005271380.1:p.Glu513=
XM_005271324.5:c.1389A>G	XP_005271381.1:p.Glu463=
XM_005271325.4:c.1359A>G	XP_005271382.1:p.Glu453=
XM_005271326.4:c.1347A>G	XP_005271383.1:p.Glu449=
XM_005271327.4:c.1164A>G	XP_005271384.1:p.Glu388=
NM_001172309.2:c.1389A>G	NP_001165780.1:p.Glu463=
NM_144573.4:c.1581A>G MANE Select	NP_653174.3:p.Glu527=