Canonical Allele Identifier: CA340875006
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77929331G>A , CM000663.2:g.77929331G>A GRCh38
NC_000001.10:g.78395016G>A , CM000663.1:g.78395016G>A GRCh37
NC_000001.9:g.78167604G>A NCBI36
NG_016625.1:g.45817G>A , LRG_442:g.45817G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.880G>A MANE Select ENSP00000333938.7:p.Glu294Lys
ENST00000330010.12:c.688G>A ENSP00000327363.8:p.Glu230Lys
ENST00000334785.11:c.880G>A ENSP00000333938.7:p.Glu294Lys
ENST00000342754.5:c.579G>A
ENST00000401035.7:c.688G>A ENSP00000383814.3:p.Glu230Lys
ENST00000440324.5:c.838G>A ENSP00000411902.1:p.Glu280Lys
ENST00000464998.1:n.340G>A
NM_001172309.1:c.688G>A NP_001165780.1:p.Glu230Lys
NM_144573.3:c.880G>A , LRG_442t1:c.880G>A NP_653174.3:p.Glu294Lys
XM_005271322.2:c.880G>A XP_005271379.1:p.Glu294Lys
XM_005271323.2:c.838G>A XP_005271380.1:p.Glu280Lys
XM_005271324.3:c.688G>A XP_005271381.1:p.Glu230Lys
XM_005271325.2:c.880G>A XP_005271382.1:p.Glu294Lys
XM_005271326.2:c.646G>A XP_005271383.1:p.Glu216Lys
XM_005271327.2:c.463G>A XP_005271384.1:p.Glu155Lys
XM_005271322.4:c.880G>A XP_005271379.1:p.Glu294Lys
XM_005271323.4:c.838G>A XP_005271380.1:p.Glu280Lys
XM_005271324.5:c.688G>A XP_005271381.1:p.Glu230Lys
XM_005271325.4:c.880G>A XP_005271382.1:p.Glu294Lys
XM_005271326.4:c.646G>A XP_005271383.1:p.Glu216Lys
XM_005271327.4:c.463G>A XP_005271384.1:p.Glu155Lys
NM_001172309.2:c.688G>A NP_001165780.1:p.Glu230Lys
NM_144573.4:c.880G>A MANE Select NP_653174.3:p.Glu294Lys