Canonical Allele Identifier: CA2574166343

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942904-TGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942905_77942907del , CM000663.2:g.77942905_77942907del	GRCh38
NC_000001.10:g.78408590_78408592del , CM000663.1:g.78408590_78408592del	GRCh37
NC_000001.9:g.78181178_78181180del	NCBI36
NG_016625.1:g.59391_59393del , LRG_442:g.59391_59393del
NG_033243.2:g.41187_41189del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*76_*78del MANE Select	ENSP00000333938.7:n.*76_*78del
ENST00000330010.12:c.*76_*78del	ENSP00000327363.8:n.*76_*78del
ENST00000334785.11:c.*76_*78del	ENSP00000333938.7:n.*76_*78del
ENST00000342754.5:c.1722_1724del
ENST00000480732.2:n.1678_1680del
NM_001172309.1:c.*76_*78del	NP_001165780.1:n.*76_*78del
NM_144573.3:c.*76_*78del , LRG_442t1:c.*76_*78del	NP_653174.3:n.*76_*78del
XM_005271322.2:c.2023_2025del	XP_005271379.1:p.Asp675del
XM_005271323.2:c.1981_1983del	XP_005271380.1:p.Asp661del
XM_005271324.3:c.1831_1833del	XP_005271381.1:p.Asp611del
XM_005271325.2:c.1801_1803del	XP_005271382.1:p.Asp601del
XM_005271326.2:c.1789_1791del	XP_005271383.1:p.Asp597del
XM_005271327.2:c.1606_1608del	XP_005271384.1:p.Asp536del
XM_005271322.4:c.2023_2025del	XP_005271379.1:p.Asp675del
XM_005271323.4:c.1981_1983del	XP_005271380.1:p.Asp661del
XM_005271324.5:c.1831_1833del	XP_005271381.1:p.Asp611del
XM_005271325.4:c.1801_1803del	XP_005271382.1:p.Asp601del
XM_005271326.4:c.1789_1791del	XP_005271383.1:p.Asp597del
XM_005271327.4:c.1606_1608del	XP_005271384.1:p.Asp536del
NM_001172309.2:c.*76_*78del	NP_001165780.1:n.*76_*78del
NM_144573.4:c.*76_*78del MANE Select	NP_653174.3:n.*76_*78del