Canonical Allele Identifier: CA1177626466

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942961_77942963delinsACT , CM000663.2:g.77942961_77942963delinsACT	GRCh38
NC_000001.10:g.78408646_78408648delinsACT , CM000663.1:g.78408646_78408648delinsACT	GRCh37
NC_000001.9:g.78181234_78181236delinsACT	NCBI36
NG_016625.1:g.59447_59449delinsACT , LRG_442:g.59447_59449delinsACT
NG_033243.2:g.41131_41133delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*132_*134delinsACT MANE Select	ENSP00000333938.7:n.*132_*134delinsACT
ENST00000330010.12:c.*132_*134delinsACT	ENSP00000327363.8:n.*132_*134delinsACT
ENST00000334785.11:c.*132_*134delinsACT	ENSP00000333938.7:n.*132_*134delinsACT
ENST00000342754.5:c.1778_1780delinsACT
ENST00000480732.2:n.1734_1736delinsACT
NM_001172309.1:c.*132_*134delinsACT	NP_001165780.1:n.*132_*134delinsACT
NM_144573.3:c.*132_*134delinsACT , LRG_442t1:c.*132_*134delinsACT	NP_653174.3:n.*132_*134delinsACT
XM_005271322.2:c.*48_*50delinsACT	XP_005271379.1:n.*48_*50delinsACT
XM_005271323.2:c.*48_*50delinsACT	XP_005271380.1:n.*48_*50delinsACT
XM_005271324.3:c.*48_*50delinsACT	XP_005271381.1:n.*48_*50delinsACT
XM_005271325.2:c.*48_*50delinsACT	XP_005271382.1:n.*48_*50delinsACT
XM_005271326.2:c.*48_*50delinsACT	XP_005271383.1:n.*48_*50delinsACT
XM_005271327.2:c.*48_*50delinsACT	XP_005271384.1:n.*48_*50delinsACT
XM_005271322.4:c.*48_*50delinsACT	XP_005271379.1:n.*48_*50delinsACT
XM_005271323.4:c.*48_*50delinsACT	XP_005271380.1:n.*48_*50delinsACT
XM_005271324.5:c.*48_*50delinsACT	XP_005271381.1:n.*48_*50delinsACT
XM_005271325.4:c.*48_*50delinsACT	XP_005271382.1:n.*48_*50delinsACT
XM_005271326.4:c.*48_*50delinsACT	XP_005271383.1:n.*48_*50delinsACT
XM_005271327.4:c.*48_*50delinsACT	XP_005271384.1:n.*48_*50delinsACT
NM_001172309.2:c.*132_*134delinsACT	NP_001165780.1:n.*132_*134delinsACT
NM_144573.4:c.*132_*134delinsACT MANE Select	NP_653174.3:n.*132_*134delinsACT