Canonical Allele Identifier: CA918893

Gene: NEXN

Linked Data

• dbSNP Id: rs759636433
• ExAC: 1:78401768 AATG / A
• gnomAD v2: 1-78401768-AATG-A
• gnomAD v3: 1-77936083-AATG-A
• gnomAD v4: 1-77936083-AATG-A
• MyVariant Identifiers: chr1:g.78401769_78401771del (hg19) ; chr1:g.77936084_77936086del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936086_77936088del , CM000663.2:g.77936086_77936088del	GRCh38
NC_000001.10:g.78401771_78401773del , CM000663.1:g.78401771_78401773del	GRCh37
NC_000001.9:g.78174359_78174361del	NCBI36
NG_016625.1:g.52572_52574del , LRG_442:g.52572_52574del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+42_1473+44del MANE Select	ENSP00000333938.7:n.1473+42_1473+44del
ENST00000330010.12:c.1281+42_1281+44del	ENSP00000327363.8:n.1281+42_1281+44del
ENST00000334785.11:c.1473+42_1473+44del	ENSP00000333938.7:n.1473+42_1473+44del
ENST00000342754.5:c.1172+42_1172+44del
ENST00000480732.2:n.1047+42_1047+44del
NM_001172309.1:c.1281+42_1281+44del	NP_001165780.1:n.1281+42_1281+44del
NM_144573.3:c.1473+42_1473+44del , LRG_442t1:c.1473+42_1473+44del	NP_653174.3:n.1473+42_1473+44del
XM_005271322.2:c.1473+42_1473+44del	XP_005271379.1:n.1473+42_1473+44del
XM_005271323.2:c.1431+42_1431+44del	XP_005271380.1:n.1431+42_1431+44del
XM_005271324.3:c.1281+42_1281+44del	XP_005271381.1:n.1281+42_1281+44del
XM_005271325.2:c.1251+2607_1251+2609del	XP_005271382.1:n.1251+2607_1251+2609del
XM_005271326.2:c.1239+42_1239+44del	XP_005271383.1:n.1239+42_1239+44del
XM_005271327.2:c.1056+42_1056+44del	XP_005271384.1:n.1056+42_1056+44del
XM_005271322.4:c.1473+42_1473+44del	XP_005271379.1:n.1473+42_1473+44del
XM_005271323.4:c.1431+42_1431+44del	XP_005271380.1:n.1431+42_1431+44del
XM_005271324.5:c.1281+42_1281+44del	XP_005271381.1:n.1281+42_1281+44del
XM_005271325.4:c.1251+2607_1251+2609del	XP_005271382.1:n.1251+2607_1251+2609del
XM_005271326.4:c.1239+42_1239+44del	XP_005271383.1:n.1239+42_1239+44del
XM_005271327.4:c.1056+42_1056+44del	XP_005271384.1:n.1056+42_1056+44del
NM_001172309.2:c.1281+42_1281+44del	NP_001165780.1:n.1281+42_1281+44del
NM_144573.4:c.1473+42_1473+44del MANE Select	NP_653174.3:n.1473+42_1473+44del