Canonical Allele Identifier: CA2646274550

Gene: NEXN

Linked Data

• gnomAD v4: 1-77933516-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933516_77933517insCC , CM000663.2:g.77933516_77933517insCC	GRCh38
NC_000001.10:g.78399201_78399202insCC , CM000663.1:g.78399201_78399202insCC	GRCh37
NC_000001.9:g.78171789_78171790insCC	NCBI36
NG_016625.1:g.50002_50003insCC , LRG_442:g.50002_50003insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+37_1251+38insCC MANE Select	ENSP00000333938.7:n.1251+37_1251+38insCC
ENST00000330010.12:c.1059+37_1059+38insCC	ENSP00000327363.8:n.1059+37_1059+38insCC
ENST00000334785.11:c.1251+37_1251+38insCC	ENSP00000333938.7:n.1251+37_1251+38insCC
ENST00000342754.5:c.950+37_950+38insCC
ENST00000440324.5:c.1209+37_1209+38insCC	ENSP00000411902.1:n.1209+37_1209+38insCC
ENST00000464998.1:n.711+37_711+38insCC
ENST00000480732.2:n.825+37_825+38insCC
NM_001172309.1:c.1059+37_1059+38insCC	NP_001165780.1:n.1059+37_1059+38insCC
NM_144573.3:c.1251+37_1251+38insCC , LRG_442t1:c.1251+37_1251+38insCC	NP_653174.3:n.1251+37_1251+38insCC
XM_005271322.2:c.1251+37_1251+38insCC	XP_005271379.1:n.1251+37_1251+38insCC
XM_005271323.2:c.1209+37_1209+38insCC	XP_005271380.1:n.1209+37_1209+38insCC
XM_005271324.3:c.1059+37_1059+38insCC	XP_005271381.1:n.1059+37_1059+38insCC
XM_005271325.2:c.1251+37_1251+38insCC	XP_005271382.1:n.1251+37_1251+38insCC
XM_005271326.2:c.1017+37_1017+38insCC	XP_005271383.1:n.1017+37_1017+38insCC
XM_005271327.2:c.834+37_834+38insCC	XP_005271384.1:n.834+37_834+38insCC
XM_005271322.4:c.1251+37_1251+38insCC	XP_005271379.1:n.1251+37_1251+38insCC
XM_005271323.4:c.1209+37_1209+38insCC	XP_005271380.1:n.1209+37_1209+38insCC
XM_005271324.5:c.1059+37_1059+38insCC	XP_005271381.1:n.1059+37_1059+38insCC
XM_005271325.4:c.1251+37_1251+38insCC	XP_005271382.1:n.1251+37_1251+38insCC
XM_005271326.4:c.1017+37_1017+38insCC	XP_005271383.1:n.1017+37_1017+38insCC
XM_005271327.4:c.834+37_834+38insCC	XP_005271384.1:n.834+37_834+38insCC
NM_001172309.2:c.1059+37_1059+38insCC	NP_001165780.1:n.1059+37_1059+38insCC
NM_144573.4:c.1251+37_1251+38insCC MANE Select	NP_653174.3:n.1251+37_1251+38insCC