Canonical Allele Identifier: CA2739708115

Gene: NEXN

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*73G>C MANE Select	ENSP00000333938.7:n.*73G>C
ENST00000330010.12:c.*73G>C	ENSP00000327363.8:n.*73G>C
ENST00000334785.11:c.*73G>C	ENSP00000333938.7:n.*73G>C
ENST00000342754.5:c.1719G>C
ENST00000480732.2:n.1675G>C
NM_001172309.1:c.*73G>C	NP_001165780.1:n.*73G>C
NM_144573.3:c.*73G>C , LRG_442t1:c.*73G>C	NP_653174.3:n.*73G>C
XM_005271322.2:c.2020G>C	XP_005271379.1:p.Asp674His
XM_005271323.2:c.1978G>C	XP_005271380.1:p.Asp660His
XM_005271324.3:c.1828G>C	XP_005271381.1:p.Asp610His
XM_005271325.2:c.1798G>C	XP_005271382.1:p.Asp600His
XM_005271326.2:c.1786G>C	XP_005271383.1:p.Asp596His
XM_005271327.2:c.1603G>C	XP_005271384.1:p.Asp535His
XM_005271322.4:c.2020G>C	XP_005271379.1:p.Asp674His
XM_005271323.4:c.1978G>C	XP_005271380.1:p.Asp660His
XM_005271324.5:c.1828G>C	XP_005271381.1:p.Asp610His
XM_005271325.4:c.1798G>C	XP_005271382.1:p.Asp600His
XM_005271326.4:c.1786G>C	XP_005271383.1:p.Asp596His
XM_005271327.4:c.1603G>C	XP_005271384.1:p.Asp535His
NM_001172309.2:c.*73G>C	NP_001165780.1:n.*73G>C
NM_144573.4:c.*73G>C MANE Select	NP_653174.3:n.*73G>C