Canonical Allele Identifier: CA340882613

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942587A>C , CM000663.2:g.77942587A>C	GRCh38
NC_000001.10:g.78408272A>C , CM000663.1:g.78408272A>C	GRCh37
NC_000001.9:g.78180860A>C	NCBI36
NG_016625.1:g.59073A>C , LRG_442:g.59073A>C
NG_033243.2:g.41507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1786A>C MANE Select	ENSP00000333938.7:p.Ser596Arg
ENST00000330010.12:c.1594A>C	ENSP00000327363.8:p.Ser532Arg
ENST00000334785.11:c.1786A>C	ENSP00000333938.7:p.Ser596Arg
ENST00000342754.5:c.1485A>C
ENST00000470735.1:n.625A>C
ENST00000480732.2:n.1360A>C
NM_001172309.1:c.1594A>C	NP_001165780.1:p.Ser532Arg
NM_144573.3:c.1786A>C , LRG_442t1:c.1786A>C	NP_653174.3:p.Ser596Arg
XM_005271322.2:c.1786A>C	XP_005271379.1:p.Ser596Arg
XM_005271323.2:c.1744A>C	XP_005271380.1:p.Ser582Arg
XM_005271324.3:c.1594A>C	XP_005271381.1:p.Ser532Arg
XM_005271325.2:c.1564A>C	XP_005271382.1:p.Ser522Arg
XM_005271326.2:c.1552A>C	XP_005271383.1:p.Ser518Arg
XM_005271327.2:c.1369A>C	XP_005271384.1:p.Ser457Arg
XM_005271322.4:c.1786A>C	XP_005271379.1:p.Ser596Arg
XM_005271323.4:c.1744A>C	XP_005271380.1:p.Ser582Arg
XM_005271324.5:c.1594A>C	XP_005271381.1:p.Ser532Arg
XM_005271325.4:c.1564A>C	XP_005271382.1:p.Ser522Arg
XM_005271326.4:c.1552A>C	XP_005271383.1:p.Ser518Arg
XM_005271327.4:c.1369A>C	XP_005271384.1:p.Ser457Arg
NM_001172309.2:c.1594A>C	NP_001165780.1:p.Ser532Arg
NM_144573.4:c.1786A>C MANE Select	NP_653174.3:p.Ser596Arg