Canonical Allele Identifier: CA1177620086
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77917505T= , CM000663.2:g.77917505T= GRCh38
NC_000001.10:g.78383190T= , CM000663.1:g.78383190T= GRCh37
NC_000001.9:g.78155778T= NCBI36
NG_016625.1:g.33991T= , LRG_442:g.33991T=

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.28-61T= MANE Select ENSP00000333938.7:n.28-61T=
ENST00000330010.12:c.28-455T= ENSP00000327363.8:n.28-455T=
ENST00000334785.11:c.28-61T= ENSP00000333938.7:n.28-61T=
ENST00000401035.7:c.28-455T= ENSP00000383814.3:n.28-455T=
ENST00000440324.5:c.28-61T= ENSP00000411902.1:n.28-61T=
NM_001172309.1:c.28-455T= NP_001165780.1:n.28-455T=
NM_144573.3:c.28-61T= , LRG_442t1:c.28-61T= NP_653174.3:n.28-61T=
XM_005271322.2:c.28-61T= XP_005271379.1:n.28-61T=
XM_005271323.2:c.28-61T= XP_005271380.1:n.28-61T=
XM_005271324.3:c.28-455T= XP_005271381.1:n.28-455T=
XM_005271325.2:c.28-61T= XP_005271382.1:n.28-61T=
XM_005271326.2:c.28-455T= XP_005271383.1:n.28-455T=
XM_005271327.2:c.28-61T= XP_005271384.1:n.28-61T=
XM_005271322.4:c.28-61T= XP_005271379.1:n.28-61T=
XM_005271323.4:c.28-61T= XP_005271380.1:n.28-61T=
XM_005271324.5:c.28-455T= XP_005271381.1:n.28-455T=
XM_005271325.4:c.28-61T= XP_005271382.1:n.28-61T=
XM_005271326.4:c.28-455T= XP_005271383.1:n.28-455T=
XM_005271327.4:c.28-61T= XP_005271384.1:n.28-61T=
NM_001172309.2:c.28-455T= NP_001165780.1:n.28-455T=
NM_144573.4:c.28-61T= MANE Select NP_653174.3:n.28-61T=