Canonical Allele Identifier: CA340878522

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401565T>G (hg19) ; chr1:g.77935880T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935880T>G , CM000663.2:g.77935880T>G	GRCh38
NC_000001.10:g.78401565T>G , CM000663.1:g.78401565T>G	GRCh37
NC_000001.9:g.78174153T>G	NCBI36
NG_016625.1:g.52366T>G , LRG_442:g.52366T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1309T>G MANE Select	ENSP00000333938.7:p.Leu437Val
ENST00000330010.12:c.1117T>G	ENSP00000327363.8:p.Leu373Val
ENST00000334785.11:c.1309T>G	ENSP00000333938.7:p.Leu437Val
ENST00000342754.5:c.1008T>G
ENST00000440324.5:c.1267T>G	ENSP00000411902.1:p.Leu423Val
ENST00000464998.1:n.769T>G
ENST00000480732.2:n.883T>G
NM_001172309.1:c.1117T>G	NP_001165780.1:p.Leu373Val
NM_144573.3:c.1309T>G , LRG_442t1:c.1309T>G	NP_653174.3:p.Leu437Val
XM_005271322.2:c.1309T>G	XP_005271379.1:p.Leu437Val
XM_005271323.2:c.1267T>G	XP_005271380.1:p.Leu423Val
XM_005271324.3:c.1117T>G	XP_005271381.1:p.Leu373Val
XM_005271325.2:c.1251+2401T>G	XP_005271382.1:n.1251+2401T>G
XM_005271326.2:c.1075T>G	XP_005271383.1:p.Leu359Val
XM_005271327.2:c.892T>G	XP_005271384.1:p.Leu298Val
XM_005271322.4:c.1309T>G	XP_005271379.1:p.Leu437Val
XM_005271323.4:c.1267T>G	XP_005271380.1:p.Leu423Val
XM_005271324.5:c.1117T>G	XP_005271381.1:p.Leu373Val
XM_005271325.4:c.1251+2401T>G	XP_005271382.1:n.1251+2401T>G
XM_005271326.4:c.1075T>G	XP_005271383.1:p.Leu359Val
XM_005271327.4:c.892T>G	XP_005271384.1:p.Leu298Val
NM_001172309.2:c.1117T>G	NP_001165780.1:p.Leu373Val
NM_144573.4:c.1309T>G MANE Select	NP_653174.3:p.Leu437Val