Canonical Allele Identifier: CA340881166

Gene: NEXN

Linked Data

• dbSNP Id: rs1180199844
• gnomAD v2: 1-78407812-A-C
• gnomAD v4: 1-77942127-A-C
• MyVariant Identifiers: chr1:g.78407812A>C (hg19) ; chr1:g.77942127A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942127A>C , CM000663.2:g.77942127A>C	GRCh38
NC_000001.10:g.78407812A>C , CM000663.1:g.78407812A>C	GRCh37
NC_000001.9:g.78180400A>C	NCBI36
NG_016625.1:g.58613A>C , LRG_442:g.58613A>C
NG_033243.2:g.41967T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1578A>C MANE Select	ENSP00000333938.7:p.Glu526Asp
ENST00000330010.12:c.1386A>C	ENSP00000327363.8:p.Glu462Asp
ENST00000334785.11:c.1578A>C	ENSP00000333938.7:p.Glu526Asp
ENST00000342754.5:c.1277A>C
ENST00000470735.1:n.417A>C
ENST00000480732.2:n.1152A>C
NM_001172309.1:c.1386A>C	NP_001165780.1:p.Glu462Asp
NM_144573.3:c.1578A>C , LRG_442t1:c.1578A>C	NP_653174.3:p.Glu526Asp
XM_005271322.2:c.1578A>C	XP_005271379.1:p.Glu526Asp
XM_005271323.2:c.1536A>C	XP_005271380.1:p.Glu512Asp
XM_005271324.3:c.1386A>C	XP_005271381.1:p.Glu462Asp
XM_005271325.2:c.1356A>C	XP_005271382.1:p.Glu452Asp
XM_005271326.2:c.1344A>C	XP_005271383.1:p.Glu448Asp
XM_005271327.2:c.1161A>C	XP_005271384.1:p.Glu387Asp
XM_005271322.4:c.1578A>C	XP_005271379.1:p.Glu526Asp
XM_005271323.4:c.1536A>C	XP_005271380.1:p.Glu512Asp
XM_005271324.5:c.1386A>C	XP_005271381.1:p.Glu462Asp
XM_005271325.4:c.1356A>C	XP_005271382.1:p.Glu452Asp
XM_005271326.4:c.1344A>C	XP_005271383.1:p.Glu448Asp
XM_005271327.4:c.1161A>C	XP_005271384.1:p.Glu387Asp
NM_001172309.2:c.1386A>C	NP_001165780.1:p.Glu462Asp
NM_144573.4:c.1578A>C MANE Select	NP_653174.3:p.Glu526Asp