Canonical Allele Identifier: CA2574166358

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942989-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942995dup , CM000663.2:g.77942995dup	GRCh38
NC_000001.10:g.78408680dup , CM000663.1:g.78408680dup	GRCh37
NC_000001.9:g.78181268dup	NCBI36
NG_016625.1:g.59481dup , LRG_442:g.59481dup
NG_033243.2:g.41104dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*166dup MANE Select	ENSP00000333938.7:n.*166dup
ENST00000330010.12:c.*166dup	ENSP00000327363.8:n.*166dup
ENST00000334785.11:c.*166dup	ENSP00000333938.7:n.*166dup
ENST00000342754.5:c.1812dup
ENST00000480732.2:n.1768dup
NM_001172309.1:c.*166dup	NP_001165780.1:n.*166dup
NM_144573.3:c.*166dup , LRG_442t1:c.*166dup	NP_653174.3:n.*166dup
XM_005271322.2:c.*82dup	XP_005271379.1:n.*82dup
XM_005271323.2:c.*82dup	XP_005271380.1:n.*82dup
XM_005271324.3:c.*82dup	XP_005271381.1:n.*82dup
XM_005271325.2:c.*82dup	XP_005271382.1:n.*82dup
XM_005271326.2:c.*82dup	XP_005271383.1:n.*82dup
XM_005271327.2:c.*82dup	XP_005271384.1:n.*82dup
XM_005271322.4:c.*82dup	XP_005271379.1:n.*82dup
XM_005271323.4:c.*82dup	XP_005271380.1:n.*82dup
XM_005271324.5:c.*82dup	XP_005271381.1:n.*82dup
XM_005271325.4:c.*82dup	XP_005271382.1:n.*82dup
XM_005271326.4:c.*82dup	XP_005271383.1:n.*82dup
XM_005271327.4:c.*82dup	XP_005271384.1:n.*82dup
NM_001172309.2:c.*166dup	NP_001165780.1:n.*166dup
NM_144573.4:c.*166dup MANE Select	NP_653174.3:n.*166dup