Canonical Allele Identifier: CA340883715

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408486G>C (hg19) ; chr1:g.77942801G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942801G>C , CM000663.2:g.77942801G>C	GRCh38
NC_000001.10:g.78408486G>C , CM000663.1:g.78408486G>C	GRCh37
NC_000001.9:g.78181074G>C	NCBI36
NG_016625.1:g.59287G>C , LRG_442:g.59287G>C
NG_033243.2:g.41293C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.2000G>C MANE Select	ENSP00000333938.7:p.Cys667Ser
ENST00000330010.12:c.1808G>C	ENSP00000327363.8:p.Cys603Ser
ENST00000334785.11:c.2000G>C	ENSP00000333938.7:p.Cys667Ser
ENST00000342754.5:c.1699G>C
ENST00000480732.2:n.1574G>C
NM_001172309.1:c.1808G>C	NP_001165780.1:p.Cys603Ser
NM_144573.3:c.2000G>C , LRG_442t1:c.2000G>C	NP_653174.3:p.Cys667Ser
XM_005271322.2:c.2000G>C	XP_005271379.1:p.Cys667Ser
XM_005271323.2:c.1958G>C	XP_005271380.1:p.Cys653Ser
XM_005271324.3:c.1808G>C	XP_005271381.1:p.Cys603Ser
XM_005271325.2:c.1778G>C	XP_005271382.1:p.Cys593Ser
XM_005271326.2:c.1766G>C	XP_005271383.1:p.Cys589Ser
XM_005271327.2:c.1583G>C	XP_005271384.1:p.Cys528Ser
XM_005271322.4:c.2000G>C	XP_005271379.1:p.Cys667Ser
XM_005271323.4:c.1958G>C	XP_005271380.1:p.Cys653Ser
XM_005271324.5:c.1808G>C	XP_005271381.1:p.Cys603Ser
XM_005271325.4:c.1778G>C	XP_005271382.1:p.Cys593Ser
XM_005271326.4:c.1766G>C	XP_005271383.1:p.Cys589Ser
XM_005271327.4:c.1583G>C	XP_005271384.1:p.Cys528Ser
NM_001172309.2:c.1808G>C	NP_001165780.1:p.Cys603Ser
NM_144573.4:c.2000G>C MANE Select	NP_653174.3:p.Cys667Ser