Canonical Allele Identifier: CA340881669

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407889A>T (hg19) ; chr1:g.77942204A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942204A>T , CM000663.2:g.77942204A>T	GRCh38
NC_000001.10:g.78407889A>T , CM000663.1:g.78407889A>T	GRCh37
NC_000001.9:g.78180477A>T	NCBI36
NG_016625.1:g.58690A>T , LRG_442:g.58690A>T
NG_033243.2:g.41890T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1655A>T MANE Select	ENSP00000333938.7:p.Gln552Leu
ENST00000330010.12:c.1463A>T	ENSP00000327363.8:p.Gln488Leu
ENST00000334785.11:c.1655A>T	ENSP00000333938.7:p.Gln552Leu
ENST00000342754.5:c.1354A>T
ENST00000470735.1:n.494A>T
ENST00000480732.2:n.1229A>T
NM_001172309.1:c.1463A>T	NP_001165780.1:p.Gln488Leu
NM_144573.3:c.1655A>T , LRG_442t1:c.1655A>T	NP_653174.3:p.Gln552Leu
XM_005271322.2:c.1655A>T	XP_005271379.1:p.Gln552Leu
XM_005271323.2:c.1613A>T	XP_005271380.1:p.Gln538Leu
XM_005271324.3:c.1463A>T	XP_005271381.1:p.Gln488Leu
XM_005271325.2:c.1433A>T	XP_005271382.1:p.Gln478Leu
XM_005271326.2:c.1421A>T	XP_005271383.1:p.Gln474Leu
XM_005271327.2:c.1238A>T	XP_005271384.1:p.Gln413Leu
XM_005271322.4:c.1655A>T	XP_005271379.1:p.Gln552Leu
XM_005271323.4:c.1613A>T	XP_005271380.1:p.Gln538Leu
XM_005271324.5:c.1463A>T	XP_005271381.1:p.Gln488Leu
XM_005271325.4:c.1433A>T	XP_005271382.1:p.Gln478Leu
XM_005271326.4:c.1421A>T	XP_005271383.1:p.Gln474Leu
XM_005271327.4:c.1238A>T	XP_005271384.1:p.Gln413Leu
NM_001172309.2:c.1463A>T	NP_001165780.1:p.Gln488Leu
NM_144573.4:c.1655A>T MANE Select	NP_653174.3:p.Gln552Leu