Canonical Allele Identifier: CA1177626841

Gene: NEXN

Linked Data

• dbSNP Id: rs1650478914

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933517_77933519del , CM000663.2:g.77933517_77933519del	GRCh38
NC_000001.10:g.78399202_78399204del , CM000663.1:g.78399202_78399204del	GRCh37
NC_000001.9:g.78171790_78171792del	NCBI36
NG_016625.1:g.50003_50005del , LRG_442:g.50003_50005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+38_1251+40del MANE Select	ENSP00000333938.7:n.1251+38_1251+40del
ENST00000330010.12:c.1059+38_1059+40del	ENSP00000327363.8:n.1059+38_1059+40del
ENST00000334785.11:c.1251+38_1251+40del	ENSP00000333938.7:n.1251+38_1251+40del
ENST00000342754.5:c.950+38_950+40del
ENST00000440324.5:c.1209+38_1209+40del	ENSP00000411902.1:n.1209+38_1209+40del
ENST00000464998.1:n.711+38_711+40del
ENST00000480732.2:n.825+38_825+40del
NM_001172309.1:c.1059+38_1059+40del	NP_001165780.1:n.1059+38_1059+40del
NM_144573.3:c.1251+38_1251+40del , LRG_442t1:c.1251+38_1251+40del	NP_653174.3:n.1251+38_1251+40del
XM_005271322.2:c.1251+38_1251+40del	XP_005271379.1:n.1251+38_1251+40del
XM_005271323.2:c.1209+38_1209+40del	XP_005271380.1:n.1209+38_1209+40del
XM_005271324.3:c.1059+38_1059+40del	XP_005271381.1:n.1059+38_1059+40del
XM_005271325.2:c.1251+38_1251+40del	XP_005271382.1:n.1251+38_1251+40del
XM_005271326.2:c.1017+38_1017+40del	XP_005271383.1:n.1017+38_1017+40del
XM_005271327.2:c.834+38_834+40del	XP_005271384.1:n.834+38_834+40del
XM_005271322.4:c.1251+38_1251+40del	XP_005271379.1:n.1251+38_1251+40del
XM_005271323.4:c.1209+38_1209+40del	XP_005271380.1:n.1209+38_1209+40del
XM_005271324.5:c.1059+38_1059+40del	XP_005271381.1:n.1059+38_1059+40del
XM_005271325.4:c.1251+38_1251+40del	XP_005271382.1:n.1251+38_1251+40del
XM_005271326.4:c.1017+38_1017+40del	XP_005271383.1:n.1017+38_1017+40del
XM_005271327.4:c.834+38_834+40del	XP_005271384.1:n.834+38_834+40del
NM_001172309.2:c.1059+38_1059+40del	NP_001165780.1:n.1059+38_1059+40del
NM_144573.4:c.1251+38_1251+40del MANE Select	NP_653174.3:n.1251+38_1251+40del