Canonical Allele Identifier: CA2739708111

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942901T>A , CM000663.2:g.77942901T>A	GRCh38
NC_000001.10:g.78408586T>A , CM000663.1:g.78408586T>A	GRCh37
NC_000001.9:g.78181174T>A	NCBI36
NG_016625.1:g.59387T>A , LRG_442:g.59387T>A
NG_033243.2:g.41193A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*72T>A MANE Select	ENSP00000333938.7:n.*72T>A
ENST00000330010.12:c.*72T>A	ENSP00000327363.8:n.*72T>A
ENST00000334785.11:c.*72T>A	ENSP00000333938.7:n.*72T>A
ENST00000342754.5:c.1718T>A
ENST00000480732.2:n.1674T>A
NM_001172309.1:c.*72T>A	NP_001165780.1:n.*72T>A
NM_144573.3:c.*72T>A , LRG_442t1:c.*72T>A	NP_653174.3:n.*72T>A
XM_005271322.2:c.2019T>A	XP_005271379.1:p.Thr673=
XM_005271323.2:c.1977T>A	XP_005271380.1:p.Thr659=
XM_005271324.3:c.1827T>A	XP_005271381.1:p.Thr609=
XM_005271325.2:c.1797T>A	XP_005271382.1:p.Thr599=
XM_005271326.2:c.1785T>A	XP_005271383.1:p.Thr595=
XM_005271327.2:c.1602T>A	XP_005271384.1:p.Thr534=
XM_005271322.4:c.2019T>A	XP_005271379.1:p.Thr673=
XM_005271323.4:c.1977T>A	XP_005271380.1:p.Thr659=
XM_005271324.5:c.1827T>A	XP_005271381.1:p.Thr609=
XM_005271325.4:c.1797T>A	XP_005271382.1:p.Thr599=
XM_005271326.4:c.1785T>A	XP_005271383.1:p.Thr595=
XM_005271327.4:c.1602T>A	XP_005271384.1:p.Thr534=
NM_001172309.2:c.*72T>A	NP_001165780.1:n.*72T>A
NM_144573.4:c.*72T>A MANE Select	NP_653174.3:n.*72T>A