Canonical Allele Identifier: CA340880917

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407766T>G (hg19) ; chr1:g.77942081T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942081T>G , CM000663.2:g.77942081T>G	GRCh38
NC_000001.10:g.78407766T>G , CM000663.1:g.78407766T>G	GRCh37
NC_000001.9:g.78180354T>G	NCBI36
NG_016625.1:g.58567T>G , LRG_442:g.58567T>G
NG_033243.2:g.42013A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1532T>G MANE Select	ENSP00000333938.7:p.Val511Gly
ENST00000330010.12:c.1340T>G	ENSP00000327363.8:p.Val447Gly
ENST00000334785.11:c.1532T>G	ENSP00000333938.7:p.Val511Gly
ENST00000342754.5:c.1231T>G
ENST00000470735.1:n.371T>G
ENST00000480732.2:n.1106T>G
NM_001172309.1:c.1340T>G	NP_001165780.1:p.Val447Gly
NM_144573.3:c.1532T>G , LRG_442t1:c.1532T>G	NP_653174.3:p.Val511Gly
XM_005271322.2:c.1532T>G	XP_005271379.1:p.Val511Gly
XM_005271323.2:c.1490T>G	XP_005271380.1:p.Val497Gly
XM_005271324.3:c.1340T>G	XP_005271381.1:p.Val447Gly
XM_005271325.2:c.1310T>G	XP_005271382.1:p.Val437Gly
XM_005271326.2:c.1298T>G	XP_005271383.1:p.Val433Gly
XM_005271327.2:c.1115T>G	XP_005271384.1:p.Val372Gly
XM_005271322.4:c.1532T>G	XP_005271379.1:p.Val511Gly
XM_005271323.4:c.1490T>G	XP_005271380.1:p.Val497Gly
XM_005271324.5:c.1340T>G	XP_005271381.1:p.Val447Gly
XM_005271325.4:c.1310T>G	XP_005271382.1:p.Val437Gly
XM_005271326.4:c.1298T>G	XP_005271383.1:p.Val433Gly
XM_005271327.4:c.1115T>G	XP_005271384.1:p.Val372Gly
NM_001172309.2:c.1340T>G	NP_001165780.1:p.Val447Gly
NM_144573.4:c.1532T>G MANE Select	NP_653174.3:p.Val511Gly