Canonical Allele Identifier: CA2696407863

Gene: NEXN

Linked Data

• dbSNP Id: rs2102147681

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933600_77933601del , CM000663.2:g.77933600_77933601del	GRCh38
NC_000001.10:g.78399285_78399286del , CM000663.1:g.78399285_78399286del	GRCh37
NC_000001.9:g.78171873_78171874del	NCBI36
NG_016625.1:g.50086_50087del , LRG_442:g.50086_50087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+121_1251+122del MANE Select	ENSP00000333938.7:n.1251+121_1251+122del
ENST00000330010.12:c.1059+121_1059+122del	ENSP00000327363.8:n.1059+121_1059+122del
ENST00000334785.11:c.1251+121_1251+122del	ENSP00000333938.7:n.1251+121_1251+122del
ENST00000342754.5:c.950+121_950+122del
ENST00000440324.5:c.1209+121_1209+122del	ENSP00000411902.1:n.1209+121_1209+122del
ENST00000464998.1:n.711+121_711+122del
ENST00000480732.2:n.825+121_825+122del
NM_001172309.1:c.1059+121_1059+122del	NP_001165780.1:n.1059+121_1059+122del
NM_144573.3:c.1251+121_1251+122del , LRG_442t1:c.1251+121_1251+122del	NP_653174.3:n.1251+121_1251+122del
XM_005271322.2:c.1251+121_1251+122del	XP_005271379.1:n.1251+121_1251+122del
XM_005271323.2:c.1209+121_1209+122del	XP_005271380.1:n.1209+121_1209+122del
XM_005271324.3:c.1059+121_1059+122del	XP_005271381.1:n.1059+121_1059+122del
XM_005271325.2:c.1251+121_1251+122del	XP_005271382.1:n.1251+121_1251+122del
XM_005271326.2:c.1017+121_1017+122del	XP_005271383.1:n.1017+121_1017+122del
XM_005271327.2:c.834+121_834+122del	XP_005271384.1:n.834+121_834+122del
XM_005271322.4:c.1251+121_1251+122del	XP_005271379.1:n.1251+121_1251+122del
XM_005271323.4:c.1209+121_1209+122del	XP_005271380.1:n.1209+121_1209+122del
XM_005271324.5:c.1059+121_1059+122del	XP_005271381.1:n.1059+121_1059+122del
XM_005271325.4:c.1251+121_1251+122del	XP_005271382.1:n.1251+121_1251+122del
XM_005271326.4:c.1017+121_1017+122del	XP_005271383.1:n.1017+121_1017+122del
XM_005271327.4:c.834+121_834+122del	XP_005271384.1:n.834+121_834+122del
NM_001172309.2:c.1059+121_1059+122del	NP_001165780.1:n.1059+121_1059+122del
NM_144573.4:c.1251+121_1251+122del MANE Select	NP_653174.3:n.1251+121_1251+122del