Canonical Allele Identifier: CA340881029

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407791A>C (hg19) ; chr1:g.77942106A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942106A>C , CM000663.2:g.77942106A>C	GRCh38
NC_000001.10:g.78407791A>C , CM000663.1:g.78407791A>C	GRCh37
NC_000001.9:g.78180379A>C	NCBI36
NG_016625.1:g.58592A>C , LRG_442:g.58592A>C
NG_033243.2:g.41988T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1557A>C MANE Select	ENSP00000333938.7:p.Gln519His
ENST00000330010.12:c.1365A>C	ENSP00000327363.8:p.Gln455His
ENST00000334785.11:c.1557A>C	ENSP00000333938.7:p.Gln519His
ENST00000342754.5:c.1256A>C
ENST00000470735.1:n.396A>C
ENST00000480732.2:n.1131A>C
NM_001172309.1:c.1365A>C	NP_001165780.1:p.Gln455His
NM_144573.3:c.1557A>C , LRG_442t1:c.1557A>C	NP_653174.3:p.Gln519His
XM_005271322.2:c.1557A>C	XP_005271379.1:p.Gln519His
XM_005271323.2:c.1515A>C	XP_005271380.1:p.Gln505His
XM_005271324.3:c.1365A>C	XP_005271381.1:p.Gln455His
XM_005271325.2:c.1335A>C	XP_005271382.1:p.Gln445His
XM_005271326.2:c.1323A>C	XP_005271383.1:p.Gln441His
XM_005271327.2:c.1140A>C	XP_005271384.1:p.Gln380His
XM_005271322.4:c.1557A>C	XP_005271379.1:p.Gln519His
XM_005271323.4:c.1515A>C	XP_005271380.1:p.Gln505His
XM_005271324.5:c.1365A>C	XP_005271381.1:p.Gln455His
XM_005271325.4:c.1335A>C	XP_005271382.1:p.Gln445His
XM_005271326.4:c.1323A>C	XP_005271383.1:p.Gln441His
XM_005271327.4:c.1140A>C	XP_005271384.1:p.Gln380His
NM_001172309.2:c.1365A>C	NP_001165780.1:p.Gln455His
NM_144573.4:c.1557A>C MANE Select	NP_653174.3:p.Gln519His