Canonical Allele Identifier: CA523842812

Gene: NEXN

Linked Data

• dbSNP Id: rs1557999236
• gnomAD v2: 1-78408574-CTCT-C
• gnomAD v4: 1-77942889-CTCT-C
• MyVariant Identifiers: chr1:g.78408576_78408578del (hg19) ; chr1:g.77942891_77942893del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942891_77942893del , CM000663.2:g.77942891_77942893del	GRCh38
NC_000001.10:g.78408576_78408578del , CM000663.1:g.78408576_78408578del	GRCh37
NC_000001.9:g.78181164_78181166del	NCBI36
NG_016625.1:g.59377_59379del , LRG_442:g.59377_59379del
NG_033243.2:g.41202_41204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*62_*64del MANE Select	ENSP00000333938.7:n.*62_*64del
ENST00000330010.12:c.*62_*64del	ENSP00000327363.8:n.*62_*64del
ENST00000334785.11:c.*62_*64del	ENSP00000333938.7:n.*62_*64del
ENST00000342754.5:c.1717-9_1717-7del
ENST00000480732.2:n.1664_1666del
NM_001172309.1:c.*62_*64del	NP_001165780.1:n.*62_*64del
NM_144573.3:c.*62_*64del , LRG_442t1:c.*62_*64del	NP_653174.3:n.*62_*64del
XM_005271322.2:c.2018-9_2018-7del	XP_005271379.1:n.2018-9_2018-7del
XM_005271323.2:c.1976-9_1976-7del	XP_005271380.1:n.1976-9_1976-7del
XM_005271324.3:c.1826-9_1826-7del	XP_005271381.1:n.1826-9_1826-7del
XM_005271325.2:c.1796-9_1796-7del	XP_005271382.1:n.1796-9_1796-7del
XM_005271326.2:c.1784-9_1784-7del	XP_005271383.1:n.1784-9_1784-7del
XM_005271327.2:c.1601-9_1601-7del	XP_005271384.1:n.1601-9_1601-7del
XM_005271322.4:c.2018-9_2018-7del	XP_005271379.1:n.2018-9_2018-7del
XM_005271323.4:c.1976-9_1976-7del	XP_005271380.1:n.1976-9_1976-7del
XM_005271324.5:c.1826-9_1826-7del	XP_005271381.1:n.1826-9_1826-7del
XM_005271325.4:c.1796-9_1796-7del	XP_005271382.1:n.1796-9_1796-7del
XM_005271326.4:c.1784-9_1784-7del	XP_005271383.1:n.1784-9_1784-7del
XM_005271327.4:c.1601-9_1601-7del	XP_005271384.1:n.1601-9_1601-7del
NM_001172309.2:c.*62_*64del	NP_001165780.1:n.*62_*64del
NM_144573.4:c.*62_*64del MANE Select	NP_653174.3:n.*62_*64del