Canonical Allele Identifier: CA739053612

Gene: NEXN

Linked Data

• dbSNP Id: rs1208809270
• MyVariant Identifiers: chr1:g.78399276_78399277insTAT (hg19) ; chr1:g.77933591_77933592insTAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933595_77933597dup , CM000663.2:g.77933595_77933597dup	GRCh38
NC_000001.10:g.78399280_78399282dup , CM000663.1:g.78399280_78399282dup	GRCh37
NC_000001.9:g.78171868_78171870dup	NCBI36
NG_016625.1:g.50081_50083dup , LRG_442:g.50081_50083dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+116_1251+118dup MANE Select	ENSP00000333938.7:n.1251+116_1251+118dup
ENST00000330010.12:c.1059+116_1059+118dup	ENSP00000327363.8:n.1059+116_1059+118dup
ENST00000334785.11:c.1251+116_1251+118dup	ENSP00000333938.7:n.1251+116_1251+118dup
ENST00000342754.5:c.950+116_950+118dup
ENST00000440324.5:c.1209+116_1209+118dup	ENSP00000411902.1:n.1209+116_1209+118dup
ENST00000464998.1:n.711+116_711+118dup
ENST00000480732.2:n.825+116_825+118dup
NM_001172309.1:c.1059+116_1059+118dup	NP_001165780.1:n.1059+116_1059+118dup
NM_144573.3:c.1251+116_1251+118dup , LRG_442t1:c.1251+116_1251+118dup	NP_653174.3:n.1251+116_1251+118dup
XM_005271322.2:c.1251+116_1251+118dup	XP_005271379.1:n.1251+116_1251+118dup
XM_005271323.2:c.1209+116_1209+118dup	XP_005271380.1:n.1209+116_1209+118dup
XM_005271324.3:c.1059+116_1059+118dup	XP_005271381.1:n.1059+116_1059+118dup
XM_005271325.2:c.1251+116_1251+118dup	XP_005271382.1:n.1251+116_1251+118dup
XM_005271326.2:c.1017+116_1017+118dup	XP_005271383.1:n.1017+116_1017+118dup
XM_005271327.2:c.834+116_834+118dup	XP_005271384.1:n.834+116_834+118dup
XM_005271322.4:c.1251+116_1251+118dup	XP_005271379.1:n.1251+116_1251+118dup
XM_005271323.4:c.1209+116_1209+118dup	XP_005271380.1:n.1209+116_1209+118dup
XM_005271324.5:c.1059+116_1059+118dup	XP_005271381.1:n.1059+116_1059+118dup
XM_005271325.4:c.1251+116_1251+118dup	XP_005271382.1:n.1251+116_1251+118dup
XM_005271326.4:c.1017+116_1017+118dup	XP_005271383.1:n.1017+116_1017+118dup
XM_005271327.4:c.834+116_834+118dup	XP_005271384.1:n.834+116_834+118dup
NM_001172309.2:c.1059+116_1059+118dup	NP_001165780.1:n.1059+116_1059+118dup
NM_144573.4:c.1251+116_1251+118dup MANE Select	NP_653174.3:n.1251+116_1251+118dup