Canonical Allele Identifier: CA919041

Gene: NEXN

Linked Data

• dbSNP Id: rs770778380
• ExAC: 1:78408565 TTTC / T
• gnomAD v2: 1-78408565-TTTC-T
• gnomAD v3: 1-77942880-TTTC-T
• gnomAD v4: 1-77942880-TTTC-T
• MyVariant Identifiers: chr1:g.78408566_78408568del (hg19) ; chr1:g.77942882_77942884del (hg38) ; chr1:g.77942881_77942883del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942888_77942890del , CM000663.2:g.77942888_77942890del	GRCh38
NC_000001.10:g.78408573_78408575del , CM000663.1:g.78408573_78408575del	GRCh37
NC_000001.9:g.78181161_78181163del	NCBI36
NG_016625.1:g.59374_59376del , LRG_442:g.59374_59376del
NG_033243.2:g.41211_41213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*59_*61del MANE Select	ENSP00000333938.7:n.*59_*61del
ENST00000330010.12:c.*59_*61del	ENSP00000327363.8:n.*59_*61del
ENST00000334785.11:c.*59_*61del	ENSP00000333938.7:n.*59_*61del
ENST00000342754.5:c.1717-12_1717-10del
ENST00000480732.2:n.1661_1663del
NM_001172309.1:c.*59_*61del	NP_001165780.1:n.*59_*61del
NM_144573.3:c.*59_*61del , LRG_442t1:c.*59_*61del	NP_653174.3:n.*59_*61del
XM_005271322.2:c.2018-12_2018-10del	XP_005271379.1:n.2018-12_2018-10del
XM_005271323.2:c.1976-12_1976-10del	XP_005271380.1:n.1976-12_1976-10del
XM_005271324.3:c.1826-12_1826-10del	XP_005271381.1:n.1826-12_1826-10del
XM_005271325.2:c.1796-12_1796-10del	XP_005271382.1:n.1796-12_1796-10del
XM_005271326.2:c.1784-12_1784-10del	XP_005271383.1:n.1784-12_1784-10del
XM_005271327.2:c.1601-12_1601-10del	XP_005271384.1:n.1601-12_1601-10del
XM_005271322.4:c.2018-12_2018-10del	XP_005271379.1:n.2018-12_2018-10del
XM_005271323.4:c.1976-12_1976-10del	XP_005271380.1:n.1976-12_1976-10del
XM_005271324.5:c.1826-12_1826-10del	XP_005271381.1:n.1826-12_1826-10del
XM_005271325.4:c.1796-12_1796-10del	XP_005271382.1:n.1796-12_1796-10del
XM_005271326.4:c.1784-12_1784-10del	XP_005271383.1:n.1784-12_1784-10del
XM_005271327.4:c.1601-12_1601-10del	XP_005271384.1:n.1601-12_1601-10del
NM_001172309.2:c.*59_*61del	NP_001165780.1:n.*59_*61del
NM_144573.4:c.*59_*61del MANE Select	NP_653174.3:n.*59_*61del