Canonical Allele Identifier: CA1177620088
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77917516C= , CM000663.2:g.77917516C= GRCh38
NC_000001.10:g.78383201C= , CM000663.1:g.78383201C= GRCh37
NC_000001.9:g.78155789C= NCBI36
NG_016625.1:g.34002C= , LRG_442:g.34002C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.28-50C= MANE Select ENSP00000333938.7:n.28-50C=
ENST00000330010.12:c.28-444C= ENSP00000327363.8:n.28-444C=
ENST00000334785.11:c.28-50C= ENSP00000333938.7:n.28-50C=
ENST00000401035.7:c.28-444C= ENSP00000383814.3:n.28-444C=
ENST00000440324.5:c.28-50C= ENSP00000411902.1:n.28-50C=
NM_001172309.1:c.28-444C= NP_001165780.1:n.28-444C=
NM_144573.3:c.28-50C= , LRG_442t1:c.28-50C= NP_653174.3:n.28-50C=
XM_005271322.2:c.28-50C= XP_005271379.1:n.28-50C=
XM_005271323.2:c.28-50C= XP_005271380.1:n.28-50C=
XM_005271324.3:c.28-444C= XP_005271381.1:n.28-444C=
XM_005271325.2:c.28-50C= XP_005271382.1:n.28-50C=
XM_005271326.2:c.28-444C= XP_005271383.1:n.28-444C=
XM_005271327.2:c.28-50C= XP_005271384.1:n.28-50C=
XM_005271322.4:c.28-50C= XP_005271379.1:n.28-50C=
XM_005271323.4:c.28-50C= XP_005271380.1:n.28-50C=
XM_005271324.5:c.28-444C= XP_005271381.1:n.28-444C=
XM_005271325.4:c.28-50C= XP_005271382.1:n.28-50C=
XM_005271326.4:c.28-444C= XP_005271383.1:n.28-444C=
XM_005271327.4:c.28-50C= XP_005271384.1:n.28-50C=
NM_001172309.2:c.28-444C= NP_001165780.1:n.28-444C=
NM_144573.4:c.28-50C= MANE Select NP_653174.3:n.28-50C=