Canonical Allele Identifier: CA340879302

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401674G>C (hg19) ; chr1:g.77935989G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935989G>C , CM000663.2:g.77935989G>C	GRCh38
NC_000001.10:g.78401674G>C , CM000663.1:g.78401674G>C	GRCh37
NC_000001.9:g.78174262G>C	NCBI36
NG_016625.1:g.52475G>C , LRG_442:g.52475G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1418G>C MANE Select	ENSP00000333938.7:p.Arg473Thr
ENST00000330010.12:c.1226G>C	ENSP00000327363.8:p.Arg409Thr
ENST00000334785.11:c.1418G>C	ENSP00000333938.7:p.Arg473Thr
ENST00000342754.5:c.1117G>C
ENST00000480732.2:n.992G>C
NM_001172309.1:c.1226G>C	NP_001165780.1:p.Arg409Thr
NM_144573.3:c.1418G>C , LRG_442t1:c.1418G>C	NP_653174.3:p.Arg473Thr
XM_005271322.2:c.1418G>C	XP_005271379.1:p.Arg473Thr
XM_005271323.2:c.1376G>C	XP_005271380.1:p.Arg459Thr
XM_005271324.3:c.1226G>C	XP_005271381.1:p.Arg409Thr
XM_005271325.2:c.1251+2510G>C	XP_005271382.1:n.1251+2510G>C
XM_005271326.2:c.1184G>C	XP_005271383.1:p.Arg395Thr
XM_005271327.2:c.1001G>C	XP_005271384.1:p.Arg334Thr
XM_005271322.4:c.1418G>C	XP_005271379.1:p.Arg473Thr
XM_005271323.4:c.1376G>C	XP_005271380.1:p.Arg459Thr
XM_005271324.5:c.1226G>C	XP_005271381.1:p.Arg409Thr
XM_005271325.4:c.1251+2510G>C	XP_005271382.1:n.1251+2510G>C
XM_005271326.4:c.1184G>C	XP_005271383.1:p.Arg395Thr
XM_005271327.4:c.1001G>C	XP_005271384.1:p.Arg334Thr
NM_001172309.2:c.1226G>C	NP_001165780.1:p.Arg409Thr
NM_144573.4:c.1418G>C MANE Select	NP_653174.3:p.Arg473Thr