Canonical Allele Identifier: CA2574413958

Gene: NEXN

Linked Data

• gnomAD v4: 1-77917522-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917524_77917525dup , CM000663.2:g.77917524_77917525dup	GRCh38
NC_000001.10:g.78383209_78383210dup , CM000663.1:g.78383209_78383210dup	GRCh37
NC_000001.9:g.78155797_78155798dup	NCBI36
NG_016625.1:g.34010_34011dup , LRG_442:g.34010_34011dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.28-42_28-41dup MANE Select	ENSP00000333938.7:n.28-42_28-41dup
ENST00000330010.12:c.28-436_28-435dup	ENSP00000327363.8:n.28-436_28-435dup
ENST00000334785.11:c.28-42_28-41dup	ENSP00000333938.7:n.28-42_28-41dup
ENST00000401035.7:c.28-436_28-435dup	ENSP00000383814.3:n.28-436_28-435dup
ENST00000440324.5:c.28-42_28-41dup	ENSP00000411902.1:n.28-42_28-41dup
NM_001172309.1:c.28-436_28-435dup	NP_001165780.1:n.28-436_28-435dup
NM_144573.3:c.28-42_28-41dup , LRG_442t1:c.28-42_28-41dup	NP_653174.3:n.28-42_28-41dup
XM_005271322.2:c.28-42_28-41dup	XP_005271379.1:n.28-42_28-41dup
XM_005271323.2:c.28-42_28-41dup	XP_005271380.1:n.28-42_28-41dup
XM_005271324.3:c.28-436_28-435dup	XP_005271381.1:n.28-436_28-435dup
XM_005271325.2:c.28-42_28-41dup	XP_005271382.1:n.28-42_28-41dup
XM_005271326.2:c.28-436_28-435dup	XP_005271383.1:n.28-436_28-435dup
XM_005271327.2:c.28-42_28-41dup	XP_005271384.1:n.28-42_28-41dup
XM_005271322.4:c.28-42_28-41dup	XP_005271379.1:n.28-42_28-41dup
XM_005271323.4:c.28-42_28-41dup	XP_005271380.1:n.28-42_28-41dup
XM_005271324.5:c.28-436_28-435dup	XP_005271381.1:n.28-436_28-435dup
XM_005271325.4:c.28-42_28-41dup	XP_005271382.1:n.28-42_28-41dup
XM_005271326.4:c.28-436_28-435dup	XP_005271383.1:n.28-436_28-435dup
XM_005271327.4:c.28-42_28-41dup	XP_005271384.1:n.28-42_28-41dup
NM_001172309.2:c.28-436_28-435dup	NP_001165780.1:n.28-436_28-435dup
NM_144573.4:c.28-42_28-41dup MANE Select	NP_653174.3:n.28-42_28-41dup