Canonical Allele Identifier: CA919044

Gene: NEXN

Linked Data

• dbSNP Id: rs751751173
• ExAC: 1:78408587 G / A
• gnomAD v2: 1-78408587-G-A
• gnomAD v4: 1-77942902-G-A
• COSMIC: COSM6389021
• MyVariant Identifiers: chr1:g.78408587G>A (hg19) ; chr1:g.77942902G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942902G>A , CM000663.2:g.77942902G>A	GRCh38
NC_000001.10:g.78408587G>A , CM000663.1:g.78408587G>A	GRCh37
NC_000001.9:g.78181175G>A	NCBI36
NG_016625.1:g.59388G>A , LRG_442:g.59388G>A
NG_033243.2:g.41192C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*73G>A MANE Select	ENSP00000333938.7:n.*73G>A
ENST00000330010.12:c.*73G>A	ENSP00000327363.8:n.*73G>A
ENST00000334785.11:c.*73G>A	ENSP00000333938.7:n.*73G>A
ENST00000342754.5:c.1719G>A
ENST00000480732.2:n.1675G>A
NM_001172309.1:c.*73G>A	NP_001165780.1:n.*73G>A
NM_144573.3:c.*73G>A , LRG_442t1:c.*73G>A	NP_653174.3:n.*73G>A
XM_005271322.2:c.2020G>A	XP_005271379.1:p.Asp674Asn
XM_005271323.2:c.1978G>A	XP_005271380.1:p.Asp660Asn
XM_005271324.3:c.1828G>A	XP_005271381.1:p.Asp610Asn
XM_005271325.2:c.1798G>A	XP_005271382.1:p.Asp600Asn
XM_005271326.2:c.1786G>A	XP_005271383.1:p.Asp596Asn
XM_005271327.2:c.1603G>A	XP_005271384.1:p.Asp535Asn
XM_005271322.4:c.2020G>A	XP_005271379.1:p.Asp674Asn
XM_005271323.4:c.1978G>A	XP_005271380.1:p.Asp660Asn
XM_005271324.5:c.1828G>A	XP_005271381.1:p.Asp610Asn
XM_005271325.4:c.1798G>A	XP_005271382.1:p.Asp600Asn
XM_005271326.4:c.1786G>A	XP_005271383.1:p.Asp596Asn
XM_005271327.4:c.1603G>A	XP_005271384.1:p.Asp535Asn
NM_001172309.2:c.*73G>A	NP_001165780.1:n.*73G>A
NM_144573.4:c.*73G>A MANE Select	NP_653174.3:n.*73G>A