Canonical Allele Identifier: CA340876571

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78398986C>G (hg19) ; chr1:g.77933301C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933301C>G , CM000663.2:g.77933301C>G	GRCh38
NC_000001.10:g.78398986C>G , CM000663.1:g.78398986C>G	GRCh37
NC_000001.9:g.78171574C>G	NCBI36
NG_016625.1:g.49787C>G , LRG_442:g.49787C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1073C>G MANE Select	ENSP00000333938.7:p.Pro358Arg
ENST00000330010.12:c.881C>G	ENSP00000327363.8:p.Pro294Arg
ENST00000334785.11:c.1073C>G	ENSP00000333938.7:p.Pro358Arg
ENST00000342754.5:c.772C>G
ENST00000401035.7:c.881C>G	ENSP00000383814.3:p.Pro294Arg
ENST00000440324.5:c.1031C>G	ENSP00000411902.1:p.Pro344Arg
ENST00000464998.1:n.533C>G
ENST00000480732.2:n.647C>G
NM_001172309.1:c.881C>G	NP_001165780.1:p.Pro294Arg
NM_144573.3:c.1073C>G , LRG_442t1:c.1073C>G	NP_653174.3:p.Pro358Arg
XM_005271322.2:c.1073C>G	XP_005271379.1:p.Pro358Arg
XM_005271323.2:c.1031C>G	XP_005271380.1:p.Pro344Arg
XM_005271324.3:c.881C>G	XP_005271381.1:p.Pro294Arg
XM_005271325.2:c.1073C>G	XP_005271382.1:p.Pro358Arg
XM_005271326.2:c.839C>G	XP_005271383.1:p.Pro280Arg
XM_005271327.2:c.656C>G	XP_005271384.1:p.Pro219Arg
XM_005271322.4:c.1073C>G	XP_005271379.1:p.Pro358Arg
XM_005271323.4:c.1031C>G	XP_005271380.1:p.Pro344Arg
XM_005271324.5:c.881C>G	XP_005271381.1:p.Pro294Arg
XM_005271325.4:c.1073C>G	XP_005271382.1:p.Pro358Arg
XM_005271326.4:c.839C>G	XP_005271383.1:p.Pro280Arg
XM_005271327.4:c.656C>G	XP_005271384.1:p.Pro219Arg
NM_001172309.2:c.881C>G	NP_001165780.1:p.Pro294Arg
NM_144573.4:c.1073C>G MANE Select	NP_653174.3:p.Pro358Arg