Canonical Allele Identifier: CA2646274611

Gene: NEXN

Linked Data

• gnomAD v4: 1-77933608-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933609_77933610insAA , CM000663.2:g.77933609_77933610insAA	GRCh38
NC_000001.10:g.78399294_78399295insAA , CM000663.1:g.78399294_78399295insAA	GRCh37
NC_000001.9:g.78171882_78171883insAA	NCBI36
NG_016625.1:g.50095_50096insAA , LRG_442:g.50095_50096insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+130_1251+131insAA MANE Select	ENSP00000333938.7:n.1251+130_1251+131insAA
ENST00000330010.12:c.1059+130_1059+131insAA	ENSP00000327363.8:n.1059+130_1059+131insAA
ENST00000334785.11:c.1251+130_1251+131insAA	ENSP00000333938.7:n.1251+130_1251+131insAA
ENST00000342754.5:c.950+130_950+131insAA
ENST00000440324.5:c.1209+130_1209+131insAA	ENSP00000411902.1:n.1209+130_1209+131insAA
ENST00000464998.1:n.711+130_711+131insAA
ENST00000480732.2:n.825+130_825+131insAA
NM_001172309.1:c.1059+130_1059+131insAA	NP_001165780.1:n.1059+130_1059+131insAA
NM_144573.3:c.1251+130_1251+131insAA , LRG_442t1:c.1251+130_1251+131insAA	NP_653174.3:n.1251+130_1251+131insAA
XM_005271322.2:c.1251+130_1251+131insAA	XP_005271379.1:n.1251+130_1251+131insAA
XM_005271323.2:c.1209+130_1209+131insAA	XP_005271380.1:n.1209+130_1209+131insAA
XM_005271324.3:c.1059+130_1059+131insAA	XP_005271381.1:n.1059+130_1059+131insAA
XM_005271325.2:c.1251+130_1251+131insAA	XP_005271382.1:n.1251+130_1251+131insAA
XM_005271326.2:c.1017+130_1017+131insAA	XP_005271383.1:n.1017+130_1017+131insAA
XM_005271327.2:c.834+130_834+131insAA	XP_005271384.1:n.834+130_834+131insAA
XM_005271322.4:c.1251+130_1251+131insAA	XP_005271379.1:n.1251+130_1251+131insAA
XM_005271323.4:c.1209+130_1209+131insAA	XP_005271380.1:n.1209+130_1209+131insAA
XM_005271324.5:c.1059+130_1059+131insAA	XP_005271381.1:n.1059+130_1059+131insAA
XM_005271325.4:c.1251+130_1251+131insAA	XP_005271382.1:n.1251+130_1251+131insAA
XM_005271326.4:c.1017+130_1017+131insAA	XP_005271383.1:n.1017+130_1017+131insAA
XM_005271327.4:c.834+130_834+131insAA	XP_005271384.1:n.834+130_834+131insAA
NM_001172309.2:c.1059+130_1059+131insAA	NP_001165780.1:n.1059+130_1059+131insAA
NM_144573.4:c.1251+130_1251+131insAA MANE Select	NP_653174.3:n.1251+130_1251+131insAA