Canonical Allele Identifier: CA2646274616

Gene: NEXN

Linked Data

• gnomAD v4: 1-77933621-TCTGCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933622_77933627del , CM000663.2:g.77933622_77933627del	GRCh38
NC_000001.10:g.78399307_78399312del , CM000663.1:g.78399307_78399312del	GRCh37
NC_000001.9:g.78171895_78171900del	NCBI36
NG_016625.1:g.50108_50113del , LRG_442:g.50108_50113del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+143_1251+148del MANE Select	ENSP00000333938.7:n.1251+143_1251+148del
ENST00000330010.12:c.1059+143_1059+148del	ENSP00000327363.8:n.1059+143_1059+148del
ENST00000334785.11:c.1251+143_1251+148del	ENSP00000333938.7:n.1251+143_1251+148del
ENST00000342754.5:c.950+143_950+148del
ENST00000440324.5:c.1209+143_1209+148del	ENSP00000411902.1:n.1209+143_1209+148del
ENST00000464998.1:n.711+143_711+148del
ENST00000480732.2:n.825+143_825+148del
NM_001172309.1:c.1059+143_1059+148del	NP_001165780.1:n.1059+143_1059+148del
NM_144573.3:c.1251+143_1251+148del , LRG_442t1:c.1251+143_1251+148del	NP_653174.3:n.1251+143_1251+148del
XM_005271322.2:c.1251+143_1251+148del	XP_005271379.1:n.1251+143_1251+148del
XM_005271323.2:c.1209+143_1209+148del	XP_005271380.1:n.1209+143_1209+148del
XM_005271324.3:c.1059+143_1059+148del	XP_005271381.1:n.1059+143_1059+148del
XM_005271325.2:c.1251+143_1251+148del	XP_005271382.1:n.1251+143_1251+148del
XM_005271326.2:c.1017+143_1017+148del	XP_005271383.1:n.1017+143_1017+148del
XM_005271327.2:c.834+143_834+148del	XP_005271384.1:n.834+143_834+148del
XM_005271322.4:c.1251+143_1251+148del	XP_005271379.1:n.1251+143_1251+148del
XM_005271323.4:c.1209+143_1209+148del	XP_005271380.1:n.1209+143_1209+148del
XM_005271324.5:c.1059+143_1059+148del	XP_005271381.1:n.1059+143_1059+148del
XM_005271325.4:c.1251+143_1251+148del	XP_005271382.1:n.1251+143_1251+148del
XM_005271326.4:c.1017+143_1017+148del	XP_005271383.1:n.1017+143_1017+148del
XM_005271327.4:c.834+143_834+148del	XP_005271384.1:n.834+143_834+148del
NM_001172309.2:c.1059+143_1059+148del	NP_001165780.1:n.1059+143_1059+148del
NM_144573.4:c.1251+143_1251+148del MANE Select	NP_653174.3:n.1251+143_1251+148del