Canonical Allele Identifier: CA739076106

Gene: NEXN

Linked Data

• dbSNP Id: rs1432075264
• gnomAD v3: 1-77917268-G-GA
• gnomAD v4: 1-77917268-G-GA
• MyVariant Identifiers: chr1:g.78382953_78382954insA (hg19) ; chr1:g.77917268_77917269insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917270dup , CM000663.2:g.77917270dup	GRCh38
NC_000001.10:g.78382955dup , CM000663.1:g.78382955dup	GRCh37
NC_000001.9:g.78155543dup	NCBI36
NG_016625.1:g.33756dup , LRG_442:g.33756dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.28-296dup MANE Select	ENSP00000333938.7:n.28-296dup
ENST00000330010.12:c.28-690dup	ENSP00000327363.8:n.28-690dup
ENST00000334785.11:c.28-296dup	ENSP00000333938.7:n.28-296dup
ENST00000401035.7:c.28-690dup	ENSP00000383814.3:n.28-690dup
ENST00000440324.5:c.28-296dup	ENSP00000411902.1:n.28-296dup
NM_001172309.1:c.28-690dup	NP_001165780.1:n.28-690dup
NM_144573.3:c.28-296dup , LRG_442t1:c.28-296dup	NP_653174.3:n.28-296dup
XM_005271322.2:c.28-296dup	XP_005271379.1:n.28-296dup
XM_005271323.2:c.28-296dup	XP_005271380.1:n.28-296dup
XM_005271324.3:c.28-690dup	XP_005271381.1:n.28-690dup
XM_005271325.2:c.28-296dup	XP_005271382.1:n.28-296dup
XM_005271326.2:c.28-690dup	XP_005271383.1:n.28-690dup
XM_005271327.2:c.28-296dup	XP_005271384.1:n.28-296dup
XM_005271322.4:c.28-296dup	XP_005271379.1:n.28-296dup
XM_005271323.4:c.28-296dup	XP_005271380.1:n.28-296dup
XM_005271324.5:c.28-690dup	XP_005271381.1:n.28-690dup
XM_005271325.4:c.28-296dup	XP_005271382.1:n.28-296dup
XM_005271326.4:c.28-690dup	XP_005271383.1:n.28-690dup
XM_005271327.4:c.28-296dup	XP_005271384.1:n.28-296dup
NM_001172309.2:c.28-690dup	NP_001165780.1:n.28-690dup
NM_144573.4:c.28-296dup MANE Select	NP_653174.3:n.28-296dup