Canonical Allele Identifier: CA739060107

Gene: NEXN

Linked Data

• dbSNP Id: rs1170756172
• gnomAD v3: 1-77943036-TC-T
• gnomAD v4: 1-77943036-TC-T
• MyVariant Identifiers: chr1:g.78408722del (hg19) ; chr1:g.77943037del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943037del , CM000663.2:g.77943037del	GRCh38
NC_000001.10:g.78408722del , CM000663.1:g.78408722del	GRCh37
NC_000001.9:g.78181310del	NCBI36
NG_016625.1:g.59523del , LRG_442:g.59523del
NG_033243.2:g.41057del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*208del MANE Select	ENSP00000333938.7:n.*208del
ENST00000330010.12:c.*208del	ENSP00000327363.8:n.*208del
ENST00000334785.11:c.*208del	ENSP00000333938.7:n.*208del
ENST00000342754.5:c.1854del
ENST00000480732.2:n.1810del
NM_001172309.1:c.*208del	NP_001165780.1:n.*208del
NM_144573.3:c.*208del , LRG_442t1:c.*208del	NP_653174.3:n.*208del
XM_005271322.2:c.*124del	XP_005271379.1:n.*124del
XM_005271323.2:c.*124del	XP_005271380.1:n.*124del
XM_005271324.3:c.*124del	XP_005271381.1:n.*124del
XM_005271325.2:c.*124del	XP_005271382.1:n.*124del
XM_005271326.2:c.*124del	XP_005271383.1:n.*124del
XM_005271327.2:c.*124del	XP_005271384.1:n.*124del
XM_005271322.4:c.*124del	XP_005271379.1:n.*124del
XM_005271323.4:c.*124del	XP_005271380.1:n.*124del
XM_005271324.5:c.*124del	XP_005271381.1:n.*124del
XM_005271325.4:c.*124del	XP_005271382.1:n.*124del
XM_005271326.4:c.*124del	XP_005271383.1:n.*124del
XM_005271327.4:c.*124del	XP_005271384.1:n.*124del
NM_001172309.2:c.*208del	NP_001165780.1:n.*208del
NM_144573.4:c.*208del MANE Select	NP_653174.3:n.*208del