Canonical Allele Identifier: CA1177626154
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942840T= , CM000663.2:g.77942840T= GRCh38
NC_000001.10:g.78408525T= , CM000663.1:g.78408525T= GRCh37
NC_000001.9:g.78181113T= NCBI36
NG_016625.1:g.59326T= , LRG_442:g.59326T=
NG_033243.2:g.41254A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.*11T= MANE Select ENSP00000333938.7:n.*11T=
ENST00000330010.12:c.*11T= ENSP00000327363.8:n.*11T=
ENST00000334785.11:c.*11T= ENSP00000333938.7:n.*11T=
ENST00000342754.5:c.1716+22T=
ENST00000480732.2:n.1613T=
NM_001172309.1:c.*11T= NP_001165780.1:n.*11T=
NM_144573.3:c.*11T= , LRG_442t1:c.*11T= NP_653174.3:n.*11T=
XM_005271322.2:c.2017+22T= XP_005271379.1:n.2017+22T=
XM_005271323.2:c.1975+22T= XP_005271380.1:n.1975+22T=
XM_005271324.3:c.1825+22T= XP_005271381.1:n.1825+22T=
XM_005271325.2:c.1795+22T= XP_005271382.1:n.1795+22T=
XM_005271326.2:c.1783+22T= XP_005271383.1:n.1783+22T=
XM_005271327.2:c.1600+22T= XP_005271384.1:n.1600+22T=
XM_005271322.4:c.2017+22T= XP_005271379.1:n.2017+22T=
XM_005271323.4:c.1975+22T= XP_005271380.1:n.1975+22T=
XM_005271324.5:c.1825+22T= XP_005271381.1:n.1825+22T=
XM_005271325.4:c.1795+22T= XP_005271382.1:n.1795+22T=
XM_005271326.4:c.1783+22T= XP_005271383.1:n.1783+22T=
XM_005271327.4:c.1600+22T= XP_005271384.1:n.1600+22T=
NM_001172309.2:c.*11T= NP_001165780.1:n.*11T=
NM_144573.4:c.*11T= MANE Select NP_653174.3:n.*11T=