Canonical Allele Identifier: CA24678822

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926831A>G , CM000663.2:g.77926831A>G	GRCh38
NC_000001.10:g.78392516A>G , CM000663.1:g.78392516A>G	GRCh37
NC_000001.9:g.78165104A>G	NCBI36
NG_016625.1:g.43317A>G , LRG_442:g.43317A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_144573.4:c.803A>G MANE Select	NP_653174.3:p.Glu268Gly
ENST00000334785.12:c.803A>G MANE Select	ENSP00000333938.7:p.Glu268Gly
NM_001172309.1:c.611A>G	NP_001165780.1:p.Glu204Gly
NM_001172309.2:c.611A>G	NP_001165780.1:p.Glu204Gly
NM_144573.3:c.803A>G , LRG_442t1:c.803A>G	NP_653174.3:p.Glu268Gly
ENST00000330010.12:c.611A>G	ENSP00000327363.8:p.Glu204Gly
ENST00000334785.11:c.803A>G	ENSP00000333938.7:p.Glu268Gly
ENST00000342754.5:c.502A>G
ENST00000401035.7:c.611A>G	ENSP00000383814.3:p.Glu204Gly
ENST00000440324.5:c.761A>G	ENSP00000411902.1:p.Glu254Gly
ENST00000464998.1:n.263A>G
XM_005271322.2:c.803A>G	XP_005271379.1:p.Glu268Gly
XM_005271322.4:c.803A>G	XP_005271379.1:p.Glu268Gly
XM_005271323.2:c.761A>G	XP_005271380.1:p.Glu254Gly
XM_005271323.4:c.761A>G	XP_005271380.1:p.Glu254Gly
XM_005271324.3:c.611A>G	XP_005271381.1:p.Glu204Gly
XM_005271324.5:c.611A>G	XP_005271381.1:p.Glu204Gly
XM_005271325.2:c.803A>G	XP_005271382.1:p.Glu268Gly
XM_005271325.4:c.803A>G	XP_005271382.1:p.Glu268Gly
XM_005271326.2:c.569A>G	XP_005271383.1:p.Glu190Gly
XM_005271326.4:c.569A>G	XP_005271383.1:p.Glu190Gly
XM_005271327.2:c.448-2485A>G	XP_005271384.1:n.448-2485A>G
XM_005271327.4:c.448-2485A>G	XP_005271384.1:n.448-2485A>G