Canonical Allele Identifier: CA2559760340

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942913dup , CM000663.2:g.77942913dup	GRCh38
NC_000001.10:g.78408598dup , CM000663.1:g.78408598dup	GRCh37
NC_000001.9:g.78181186dup	NCBI36
NG_016625.1:g.59399dup , LRG_442:g.59399dup
NG_033243.2:g.41181dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*84dup MANE Select	ENSP00000333938.7:n.*84dup
ENST00000330010.12:c.*84dup	ENSP00000327363.8:n.*84dup
ENST00000334785.11:c.*84dup	ENSP00000333938.7:n.*84dup
ENST00000342754.5:c.1730dup
ENST00000480732.2:n.1686dup
NM_001172309.1:c.*84dup	NP_001165780.1:n.*84dup
NM_144573.3:c.*84dup , LRG_442t1:c.*84dup	NP_653174.3:n.*84dup
XM_005271322.2:c.2031dup	XP_005271379.1:n.2031dup
XM_005271323.2:c.1989dup	XP_005271380.1:n.1989dup
XM_005271324.3:c.1839dup	XP_005271381.1:n.1839dup
XM_005271325.2:c.1809dup	XP_005271382.1:n.1809dup
XM_005271326.2:c.1797dup	XP_005271383.1:n.1797dup
XM_005271327.2:c.1614dup	XP_005271384.1:n.1614dup
XM_005271322.4:c.2031dup	XP_005271379.1:n.2031dup
XM_005271323.4:c.1989dup	XP_005271380.1:n.1989dup
XM_005271324.5:c.1839dup	XP_005271381.1:n.1839dup
XM_005271325.4:c.1809dup	XP_005271382.1:n.1809dup
XM_005271326.4:c.1797dup	XP_005271383.1:n.1797dup
XM_005271327.4:c.1614dup	XP_005271384.1:n.1614dup
NM_001172309.2:c.*84dup	NP_001165780.1:n.*84dup
NM_144573.4:c.*84dup MANE Select	NP_653174.3:n.*84dup