Canonical Allele Identifier: CA646064432

Gene: NEXN

Linked Data

• COSMIC: COSN17924970

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942996_77942997insA , CM000663.2:g.77942996_77942997insA	GRCh38
NC_000001.10:g.78408681_78408682insA , CM000663.1:g.78408681_78408682insA	GRCh37
NC_000001.9:g.78181269_78181270insA	NCBI36
NG_016625.1:g.59482_59483insA , LRG_442:g.59482_59483insA
NG_033243.2:g.41097_41098insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*167_*168insA MANE Select	ENSP00000333938.7:n.*167_*168insA
ENST00000330010.12:c.*167_*168insA	ENSP00000327363.8:n.*167_*168insA
ENST00000334785.11:c.*167_*168insA	ENSP00000333938.7:n.*167_*168insA
ENST00000342754.5:c.1813_1814insA
ENST00000480732.2:n.1769_1770insA
NM_001172309.1:c.*167_*168insA	NP_001165780.1:n.*167_*168insA
NM_144573.3:c.*167_*168insA , LRG_442t1:c.*167_*168insA	NP_653174.3:n.*167_*168insA
XM_005271322.2:c.*83_*84insA	XP_005271379.1:n.*83_*84insA
XM_005271323.2:c.*83_*84insA	XP_005271380.1:n.*83_*84insA
XM_005271324.3:c.*83_*84insA	XP_005271381.1:n.*83_*84insA
XM_005271325.2:c.*83_*84insA	XP_005271382.1:n.*83_*84insA
XM_005271326.2:c.*83_*84insA	XP_005271383.1:n.*83_*84insA
XM_005271327.2:c.*83_*84insA	XP_005271384.1:n.*83_*84insA
XM_005271322.4:c.*83_*84insA	XP_005271379.1:n.*83_*84insA
XM_005271323.4:c.*83_*84insA	XP_005271380.1:n.*83_*84insA
XM_005271324.5:c.*83_*84insA	XP_005271381.1:n.*83_*84insA
XM_005271325.4:c.*83_*84insA	XP_005271382.1:n.*83_*84insA
XM_005271326.4:c.*83_*84insA	XP_005271383.1:n.*83_*84insA
XM_005271327.4:c.*83_*84insA	XP_005271384.1:n.*83_*84insA
NM_001172309.2:c.*167_*168insA	NP_001165780.1:n.*167_*168insA
NM_144573.4:c.*167_*168insA MANE Select	NP_653174.3:n.*167_*168insA