Canonical Allele Identifier: CA524231117

Gene: NEXN

Linked Data

• dbSNP Id: rs1420664729
• gnomAD v2: 1-78399169-G-GAA
• MyVariant Identifiers: chr1:g.78399169_78399170insAA (hg19) ; chr1:g.77933484_77933485insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933485_77933486insAA , CM000663.2:g.77933485_77933486insAA	GRCh38
NC_000001.10:g.78399170_78399171insAA , CM000663.1:g.78399170_78399171insAA	GRCh37
NC_000001.9:g.78171758_78171759insAA	NCBI36
NG_016625.1:g.49971_49972insAA , LRG_442:g.49971_49972insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+6_1251+7insAA MANE Select	ENSP00000333938.7:n.1251+6_1251+7insAA
ENST00000330010.12:c.1059+6_1059+7insAA	ENSP00000327363.8:n.1059+6_1059+7insAA
ENST00000334785.11:c.1251+6_1251+7insAA	ENSP00000333938.7:n.1251+6_1251+7insAA
ENST00000342754.5:c.950+6_950+7insAA
ENST00000440324.5:c.1209+6_1209+7insAA	ENSP00000411902.1:n.1209+6_1209+7insAA
ENST00000464998.1:n.711+6_711+7insAA
ENST00000480732.2:n.825+6_825+7insAA
NM_001172309.1:c.1059+6_1059+7insAA	NP_001165780.1:n.1059+6_1059+7insAA
NM_144573.3:c.1251+6_1251+7insAA , LRG_442t1:c.1251+6_1251+7insAA	NP_653174.3:n.1251+6_1251+7insAA
XM_005271322.2:c.1251+6_1251+7insAA	XP_005271379.1:n.1251+6_1251+7insAA
XM_005271323.2:c.1209+6_1209+7insAA	XP_005271380.1:n.1209+6_1209+7insAA
XM_005271324.3:c.1059+6_1059+7insAA	XP_005271381.1:n.1059+6_1059+7insAA
XM_005271325.2:c.1251+6_1251+7insAA	XP_005271382.1:n.1251+6_1251+7insAA
XM_005271326.2:c.1017+6_1017+7insAA	XP_005271383.1:n.1017+6_1017+7insAA
XM_005271327.2:c.834+6_834+7insAA	XP_005271384.1:n.834+6_834+7insAA
XM_005271322.4:c.1251+6_1251+7insAA	XP_005271379.1:n.1251+6_1251+7insAA
XM_005271323.4:c.1209+6_1209+7insAA	XP_005271380.1:n.1209+6_1209+7insAA
XM_005271324.5:c.1059+6_1059+7insAA	XP_005271381.1:n.1059+6_1059+7insAA
XM_005271325.4:c.1251+6_1251+7insAA	XP_005271382.1:n.1251+6_1251+7insAA
XM_005271326.4:c.1017+6_1017+7insAA	XP_005271383.1:n.1017+6_1017+7insAA
XM_005271327.4:c.834+6_834+7insAA	XP_005271384.1:n.834+6_834+7insAA
NM_001172309.2:c.1059+6_1059+7insAA	NP_001165780.1:n.1059+6_1059+7insAA
NM_144573.4:c.1251+6_1251+7insAA MANE Select	NP_653174.3:n.1251+6_1251+7insAA