Canonical Allele Identifier: CA418573471

Gene: NEXN

Linked Data

• dbSNP Id: rs771265130
• MyVariant Identifiers: chr1:g.78407851C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942166C>T , CM000663.2:g.77942166C>T	GRCh38
NC_000001.10:g.78407851C>T , CM000663.1:g.78407851C>T	GRCh37
NC_000001.9:g.78180439C>T	NCBI36
NG_016625.1:g.58652C>T , LRG_442:g.58652C>T
NG_033243.2:g.41928G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1617C>T MANE Select	ENSP00000333938.7:p.Arg539=
ENST00000330010.12:c.1425C>T	ENSP00000327363.8:p.Arg475=
ENST00000334785.11:c.1617C>T	ENSP00000333938.7:p.Arg539=
ENST00000342754.5:c.1316C>T
ENST00000470735.1:n.456C>T
ENST00000480732.2:n.1191C>T
NM_001172309.1:c.1425C>T	NP_001165780.1:p.Arg475=
NM_144573.3:c.1617C>T , LRG_442t1:c.1617C>T	NP_653174.3:p.Arg539=
XM_005271322.2:c.1617C>T	XP_005271379.1:p.Arg539=
XM_005271323.2:c.1575C>T	XP_005271380.1:p.Arg525=
XM_005271324.3:c.1425C>T	XP_005271381.1:p.Arg475=
XM_005271325.2:c.1395C>T	XP_005271382.1:p.Arg465=
XM_005271326.2:c.1383C>T	XP_005271383.1:p.Arg461=
XM_005271327.2:c.1200C>T	XP_005271384.1:p.Arg400=
XM_005271322.4:c.1617C>T	XP_005271379.1:p.Arg539=
XM_005271323.4:c.1575C>T	XP_005271380.1:p.Arg525=
XM_005271324.5:c.1425C>T	XP_005271381.1:p.Arg475=
XM_005271325.4:c.1395C>T	XP_005271382.1:p.Arg465=
XM_005271326.4:c.1383C>T	XP_005271383.1:p.Arg461=
XM_005271327.4:c.1200C>T	XP_005271384.1:p.Arg400=
NM_001172309.2:c.1425C>T	NP_001165780.1:p.Arg475=
NM_144573.4:c.1617C>T MANE Select	NP_653174.3:p.Arg539=