Canonical Allele Identifier: CA524231126

Gene: NEXN

Linked Data

• dbSNP Id: rs1291331572
• gnomAD v2: 1-78399231-TATA-T
• gnomAD v3: 1-77933546-TATA-T
• gnomAD v4: 1-77933546-TATA-T
• MyVariant Identifiers: chr1:g.78399232_78399234del (hg19) ; chr1:g.77933547_77933549del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933551_77933553del , CM000663.2:g.77933551_77933553del	GRCh38
NC_000001.10:g.78399236_78399238del , CM000663.1:g.78399236_78399238del	GRCh37
NC_000001.9:g.78171824_78171826del	NCBI36
NG_016625.1:g.50037_50039del , LRG_442:g.50037_50039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+72_1251+74del MANE Select	ENSP00000333938.7:n.1251+72_1251+74del
ENST00000330010.12:c.1059+72_1059+74del	ENSP00000327363.8:n.1059+72_1059+74del
ENST00000334785.11:c.1251+72_1251+74del	ENSP00000333938.7:n.1251+72_1251+74del
ENST00000342754.5:c.950+72_950+74del
ENST00000440324.5:c.1209+72_1209+74del	ENSP00000411902.1:n.1209+72_1209+74del
ENST00000464998.1:n.711+72_711+74del
ENST00000480732.2:n.825+72_825+74del
NM_001172309.1:c.1059+72_1059+74del	NP_001165780.1:n.1059+72_1059+74del
NM_144573.3:c.1251+72_1251+74del , LRG_442t1:c.1251+72_1251+74del	NP_653174.3:n.1251+72_1251+74del
XM_005271322.2:c.1251+72_1251+74del	XP_005271379.1:n.1251+72_1251+74del
XM_005271323.2:c.1209+72_1209+74del	XP_005271380.1:n.1209+72_1209+74del
XM_005271324.3:c.1059+72_1059+74del	XP_005271381.1:n.1059+72_1059+74del
XM_005271325.2:c.1251+72_1251+74del	XP_005271382.1:n.1251+72_1251+74del
XM_005271326.2:c.1017+72_1017+74del	XP_005271383.1:n.1017+72_1017+74del
XM_005271327.2:c.834+72_834+74del	XP_005271384.1:n.834+72_834+74del
XM_005271322.4:c.1251+72_1251+74del	XP_005271379.1:n.1251+72_1251+74del
XM_005271323.4:c.1209+72_1209+74del	XP_005271380.1:n.1209+72_1209+74del
XM_005271324.5:c.1059+72_1059+74del	XP_005271381.1:n.1059+72_1059+74del
XM_005271325.4:c.1251+72_1251+74del	XP_005271382.1:n.1251+72_1251+74del
XM_005271326.4:c.1017+72_1017+74del	XP_005271383.1:n.1017+72_1017+74del
XM_005271327.4:c.834+72_834+74del	XP_005271384.1:n.834+72_834+74del
NM_001172309.2:c.1059+72_1059+74del	NP_001165780.1:n.1059+72_1059+74del
NM_144573.4:c.1251+72_1251+74del MANE Select	NP_653174.3:n.1251+72_1251+74del