Canonical Allele Identifier: CA24686117

Gene: NEXN

Linked Data

• dbSNP Id: rs573245103
• gnomAD v2: 1-78401266-G-GT
• gnomAD v3: 1-77935581-G-GT
• gnomAD v4: 1-77935581-G-GT
• MyVariant Identifiers: chr1:g.78401266_78401267insT (hg19) ; chr1:g.77935581_77935582insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935582dup , CM000663.2:g.77935582dup	GRCh38
NC_000001.10:g.78401267dup , CM000663.1:g.78401267dup	GRCh37
NC_000001.9:g.78173855dup	NCBI36
NG_016625.1:g.52068dup , LRG_442:g.52068dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1252-241dup MANE Select	ENSP00000333938.7:n.1252-241dup
ENST00000330010.12:c.1060-241dup	ENSP00000327363.8:n.1060-241dup
ENST00000334785.11:c.1252-241dup	ENSP00000333938.7:n.1252-241dup
ENST00000342754.5:c.951-241dup
ENST00000440324.5:c.1210-241dup	ENSP00000411902.1:n.1210-241dup
ENST00000464998.1:n.712-241dup
ENST00000480732.2:n.826-241dup
NM_001172309.1:c.1060-241dup	NP_001165780.1:n.1060-241dup
NM_144573.3:c.1252-241dup , LRG_442t1:c.1252-241dup	NP_653174.3:n.1252-241dup
XM_005271322.2:c.1252-241dup	XP_005271379.1:n.1252-241dup
XM_005271323.2:c.1210-241dup	XP_005271380.1:n.1210-241dup
XM_005271324.3:c.1060-241dup	XP_005271381.1:n.1060-241dup
XM_005271325.2:c.1251+2103dup	XP_005271382.1:n.1251+2103dup
XM_005271326.2:c.1018-241dup	XP_005271383.1:n.1018-241dup
XM_005271327.2:c.835-241dup	XP_005271384.1:n.835-241dup
XM_005271322.4:c.1252-241dup	XP_005271379.1:n.1252-241dup
XM_005271323.4:c.1210-241dup	XP_005271380.1:n.1210-241dup
XM_005271324.5:c.1060-241dup	XP_005271381.1:n.1060-241dup
XM_005271325.4:c.1251+2103dup	XP_005271382.1:n.1251+2103dup
XM_005271326.4:c.1018-241dup	XP_005271383.1:n.1018-241dup
XM_005271327.4:c.835-241dup	XP_005271384.1:n.835-241dup
NM_001172309.2:c.1060-241dup	NP_001165780.1:n.1060-241dup
NM_144573.4:c.1252-241dup MANE Select	NP_653174.3:n.1252-241dup