Canonical Allele Identifier: CA418709526

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401714T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936029T>A , CM000663.2:g.77936029T>A	GRCh38
NC_000001.10:g.78401714T>A , CM000663.1:g.78401714T>A	GRCh37
NC_000001.9:g.78174302T>A	NCBI36
NG_016625.1:g.52515T>A , LRG_442:g.52515T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1458T>A MANE Select	ENSP00000333938.7:p.Ala486=
ENST00000330010.12:c.1266T>A	ENSP00000327363.8:p.Ala422=
ENST00000334785.11:c.1458T>A	ENSP00000333938.7:p.Ala486=
ENST00000342754.5:c.1157T>A
ENST00000480732.2:n.1032T>A
NM_001172309.1:c.1266T>A	NP_001165780.1:p.Ala422=
NM_144573.3:c.1458T>A , LRG_442t1:c.1458T>A	NP_653174.3:p.Ala486=
XM_005271322.2:c.1458T>A	XP_005271379.1:p.Ala486=
XM_005271323.2:c.1416T>A	XP_005271380.1:p.Ala472=
XM_005271324.3:c.1266T>A	XP_005271381.1:p.Ala422=
XM_005271325.2:c.1251+2550T>A	XP_005271382.1:n.1251+2550T>A
XM_005271326.2:c.1224T>A	XP_005271383.1:p.Ala408=
XM_005271327.2:c.1041T>A	XP_005271384.1:p.Ala347=
XM_005271322.4:c.1458T>A	XP_005271379.1:p.Ala486=
XM_005271323.4:c.1416T>A	XP_005271380.1:p.Ala472=
XM_005271324.5:c.1266T>A	XP_005271381.1:p.Ala422=
XM_005271325.4:c.1251+2550T>A	XP_005271382.1:n.1251+2550T>A
XM_005271326.4:c.1224T>A	XP_005271383.1:p.Ala408=
XM_005271327.4:c.1041T>A	XP_005271384.1:p.Ala347=
NM_001172309.2:c.1266T>A	NP_001165780.1:p.Ala422=
NM_144573.4:c.1458T>A MANE Select	NP_653174.3:p.Ala486=