Canonical Allele Identifier: CA340872234

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926448C>G , CM000663.2:g.77926448C>G	GRCh38
NC_000001.10:g.78392133C>G , CM000663.1:g.78392133C>G	GRCh37
NC_000001.9:g.78164721C>G	NCBI36
NG_016625.1:g.42934C>G , LRG_442:g.42934C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_144573.4:c.524C>G MANE Select	NP_653174.3:p.Pro175Arg
ENST00000334785.12:c.524C>G MANE Select	ENSP00000333938.7:p.Pro175Arg
NM_001172309.1:c.332C>G	NP_001165780.1:p.Pro111Arg
NM_001172309.2:c.332C>G	NP_001165780.1:p.Pro111Arg
NM_144573.3:c.524C>G , LRG_442t1:c.524C>G	NP_653174.3:p.Pro175Arg
ENST00000330010.12:c.332C>G	ENSP00000327363.8:p.Pro111Arg
ENST00000334785.11:c.524C>G	ENSP00000333938.7:p.Pro175Arg
ENST00000342754.5:c.223C>G
ENST00000401035.7:c.332C>G	ENSP00000383814.3:p.Pro111Arg
ENST00000440324.5:c.482C>G	ENSP00000411902.1:p.Pro161Arg
XM_005271322.2:c.524C>G	XP_005271379.1:p.Pro175Arg
XM_005271322.4:c.524C>G	XP_005271379.1:p.Pro175Arg
XM_005271323.2:c.482C>G	XP_005271380.1:p.Pro161Arg
XM_005271323.4:c.482C>G	XP_005271380.1:p.Pro161Arg
XM_005271324.3:c.332C>G	XP_005271381.1:p.Pro111Arg
XM_005271324.5:c.332C>G	XP_005271381.1:p.Pro111Arg
XM_005271325.2:c.524C>G	XP_005271382.1:p.Pro175Arg
XM_005271325.4:c.524C>G	XP_005271382.1:p.Pro175Arg
XM_005271326.2:c.290C>G	XP_005271383.1:p.Pro97Arg
XM_005271326.4:c.290C>G	XP_005271383.1:p.Pro97Arg
XM_005271327.2:c.448-2868C>G	XP_005271384.1:n.448-2868C>G
XM_005271327.4:c.448-2868C>G	XP_005271384.1:n.448-2868C>G