Canonical Allele Identifier: CA340879290

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401671C>A (hg19) ; chr1:g.77935986C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935986C>A , CM000663.2:g.77935986C>A	GRCh38
NC_000001.10:g.78401671C>A , CM000663.1:g.78401671C>A	GRCh37
NC_000001.9:g.78174259C>A	NCBI36
NG_016625.1:g.52472C>A , LRG_442:g.52472C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1415C>A MANE Select	ENSP00000333938.7:p.Ala472Glu
ENST00000330010.12:c.1223C>A	ENSP00000327363.8:p.Ala408Glu
ENST00000334785.11:c.1415C>A	ENSP00000333938.7:p.Ala472Glu
ENST00000342754.5:c.1114C>A
ENST00000480732.2:n.989C>A
NM_001172309.1:c.1223C>A	NP_001165780.1:p.Ala408Glu
NM_144573.3:c.1415C>A , LRG_442t1:c.1415C>A	NP_653174.3:p.Ala472Glu
XM_005271322.2:c.1415C>A	XP_005271379.1:p.Ala472Glu
XM_005271323.2:c.1373C>A	XP_005271380.1:p.Ala458Glu
XM_005271324.3:c.1223C>A	XP_005271381.1:p.Ala408Glu
XM_005271325.2:c.1251+2507C>A	XP_005271382.1:n.1251+2507C>A
XM_005271326.2:c.1181C>A	XP_005271383.1:p.Ala394Glu
XM_005271327.2:c.998C>A	XP_005271384.1:p.Ala333Glu
XM_005271322.4:c.1415C>A	XP_005271379.1:p.Ala472Glu
XM_005271323.4:c.1373C>A	XP_005271380.1:p.Ala458Glu
XM_005271324.5:c.1223C>A	XP_005271381.1:p.Ala408Glu
XM_005271325.4:c.1251+2507C>A	XP_005271382.1:n.1251+2507C>A
XM_005271326.4:c.1181C>A	XP_005271383.1:p.Ala394Glu
XM_005271327.4:c.998C>A	XP_005271384.1:p.Ala333Glu
NM_001172309.2:c.1223C>A	NP_001165780.1:p.Ala408Glu
NM_144573.4:c.1415C>A MANE Select	NP_653174.3:p.Ala472Glu