Canonical Allele Identifier: CA1177626503

Gene: NEXN

Linked Data

• dbSNP Id: rs1651528778

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942989dup , CM000663.2:g.77942989dup	GRCh38
NC_000001.10:g.78408674dup , CM000663.1:g.78408674dup	GRCh37
NC_000001.9:g.78181262dup	NCBI36
NG_016625.1:g.59475dup , LRG_442:g.59475dup
NG_033243.2:g.41106dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*160dup MANE Select	ENSP00000333938.7:n.*160dup
ENST00000330010.12:c.*160dup	ENSP00000327363.8:n.*160dup
ENST00000334785.11:c.*160dup	ENSP00000333938.7:n.*160dup
ENST00000342754.5:c.1806dup
ENST00000480732.2:n.1762dup
NM_001172309.1:c.*160dup	NP_001165780.1:n.*160dup
NM_144573.3:c.*160dup , LRG_442t1:c.*160dup	NP_653174.3:n.*160dup
XM_005271322.2:c.*76dup	XP_005271379.1:n.*76dup
XM_005271323.2:c.*76dup	XP_005271380.1:n.*76dup
XM_005271324.3:c.*76dup	XP_005271381.1:n.*76dup
XM_005271325.2:c.*76dup	XP_005271382.1:n.*76dup
XM_005271326.2:c.*76dup	XP_005271383.1:n.*76dup
XM_005271327.2:c.*76dup	XP_005271384.1:n.*76dup
XM_005271322.4:c.*76dup	XP_005271379.1:n.*76dup
XM_005271323.4:c.*76dup	XP_005271380.1:n.*76dup
XM_005271324.5:c.*76dup	XP_005271381.1:n.*76dup
XM_005271325.4:c.*76dup	XP_005271382.1:n.*76dup
XM_005271326.4:c.*76dup	XP_005271383.1:n.*76dup
XM_005271327.4:c.*76dup	XP_005271384.1:n.*76dup
NM_001172309.2:c.*160dup	NP_001165780.1:n.*160dup
NM_144573.4:c.*160dup MANE Select	NP_653174.3:n.*160dup