Canonical Allele Identifier: CA739053606

Gene: NEXN

Linked Data

• dbSNP Id: rs1465838203
• gnomAD v3: 1-77933584-T-TTGTC
• gnomAD v4: 1-77933584-T-TTGTC
• MyVariant Identifiers: chr1:g.78399269_78399270insTGTC (hg19) ; chr1:g.77933584_77933585insTGTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933584_77933585insTGTC , CM000663.2:g.77933584_77933585insTGTC	GRCh38
NC_000001.10:g.78399269_78399270insTGTC , CM000663.1:g.78399269_78399270insTGTC	GRCh37
NC_000001.9:g.78171857_78171858insTGTC	NCBI36
NG_016625.1:g.50070_50071insTGTC , LRG_442:g.50070_50071insTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+105_1251+106insTGTC MANE Select	ENSP00000333938.7:n.1251+105_1251+106insTGTC
ENST00000330010.12:c.1059+105_1059+106insTGTC	ENSP00000327363.8:n.1059+105_1059+106insTGTC
ENST00000334785.11:c.1251+105_1251+106insTGTC	ENSP00000333938.7:n.1251+105_1251+106insTGTC
ENST00000342754.5:c.950+105_950+106insTGTC
ENST00000440324.5:c.1209+105_1209+106insTGTC	ENSP00000411902.1:n.1209+105_1209+106insTGTC
ENST00000464998.1:n.711+105_711+106insTGTC
ENST00000480732.2:n.825+105_825+106insTGTC
NM_001172309.1:c.1059+105_1059+106insTGTC	NP_001165780.1:n.1059+105_1059+106insTGTC
NM_144573.3:c.1251+105_1251+106insTGTC , LRG_442t1:c.1251+105_1251+106insTGTC	NP_653174.3:n.1251+105_1251+106insTGTC
XM_005271322.2:c.1251+105_1251+106insTGTC	XP_005271379.1:n.1251+105_1251+106insTGTC
XM_005271323.2:c.1209+105_1209+106insTGTC	XP_005271380.1:n.1209+105_1209+106insTGTC
XM_005271324.3:c.1059+105_1059+106insTGTC	XP_005271381.1:n.1059+105_1059+106insTGTC
XM_005271325.2:c.1251+105_1251+106insTGTC	XP_005271382.1:n.1251+105_1251+106insTGTC
XM_005271326.2:c.1017+105_1017+106insTGTC	XP_005271383.1:n.1017+105_1017+106insTGTC
XM_005271327.2:c.834+105_834+106insTGTC	XP_005271384.1:n.834+105_834+106insTGTC
XM_005271322.4:c.1251+105_1251+106insTGTC	XP_005271379.1:n.1251+105_1251+106insTGTC
XM_005271323.4:c.1209+105_1209+106insTGTC	XP_005271380.1:n.1209+105_1209+106insTGTC
XM_005271324.5:c.1059+105_1059+106insTGTC	XP_005271381.1:n.1059+105_1059+106insTGTC
XM_005271325.4:c.1251+105_1251+106insTGTC	XP_005271382.1:n.1251+105_1251+106insTGTC
XM_005271326.4:c.1017+105_1017+106insTGTC	XP_005271383.1:n.1017+105_1017+106insTGTC
XM_005271327.4:c.834+105_834+106insTGTC	XP_005271384.1:n.834+105_834+106insTGTC
NM_001172309.2:c.1059+105_1059+106insTGTC	NP_001165780.1:n.1059+105_1059+106insTGTC
NM_144573.4:c.1251+105_1251+106insTGTC MANE Select	NP_653174.3:n.1251+105_1251+106insTGTC