Canonical Allele Identifier: CA340881012

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407789C>G (hg19) ; chr1:g.77942104C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942104C>G , CM000663.2:g.77942104C>G	GRCh38
NC_000001.10:g.78407789C>G , CM000663.1:g.78407789C>G	GRCh37
NC_000001.9:g.78180377C>G	NCBI36
NG_016625.1:g.58590C>G , LRG_442:g.58590C>G
NG_033243.2:g.41990G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1555C>G MANE Select	ENSP00000333938.7:p.Gln519Glu
ENST00000330010.12:c.1363C>G	ENSP00000327363.8:p.Gln455Glu
ENST00000334785.11:c.1555C>G	ENSP00000333938.7:p.Gln519Glu
ENST00000342754.5:c.1254C>G
ENST00000470735.1:n.394C>G
ENST00000480732.2:n.1129C>G
NM_001172309.1:c.1363C>G	NP_001165780.1:p.Gln455Glu
NM_144573.3:c.1555C>G , LRG_442t1:c.1555C>G	NP_653174.3:p.Gln519Glu
XM_005271322.2:c.1555C>G	XP_005271379.1:p.Gln519Glu
XM_005271323.2:c.1513C>G	XP_005271380.1:p.Gln505Glu
XM_005271324.3:c.1363C>G	XP_005271381.1:p.Gln455Glu
XM_005271325.2:c.1333C>G	XP_005271382.1:p.Gln445Glu
XM_005271326.2:c.1321C>G	XP_005271383.1:p.Gln441Glu
XM_005271327.2:c.1138C>G	XP_005271384.1:p.Gln380Glu
XM_005271322.4:c.1555C>G	XP_005271379.1:p.Gln519Glu
XM_005271323.4:c.1513C>G	XP_005271380.1:p.Gln505Glu
XM_005271324.5:c.1363C>G	XP_005271381.1:p.Gln455Glu
XM_005271325.4:c.1333C>G	XP_005271382.1:p.Gln445Glu
XM_005271326.4:c.1321C>G	XP_005271383.1:p.Gln441Glu
XM_005271327.4:c.1138C>G	XP_005271384.1:p.Gln380Glu
NM_001172309.2:c.1363C>G	NP_001165780.1:p.Gln455Glu
NM_144573.4:c.1555C>G MANE Select	NP_653174.3:p.Gln519Glu