Canonical Allele Identifier: CA340874665

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78392563G>A (hg19) ; chr1:g.77926878G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926878G>A , CM000663.2:g.77926878G>A	GRCh38
NC_000001.10:g.78392563G>A , CM000663.1:g.78392563G>A	GRCh37
NC_000001.9:g.78165151G>A	NCBI36
NG_016625.1:g.43364G>A , LRG_442:g.43364G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.850G>A MANE Select	ENSP00000333938.7:p.Ala284Thr
ENST00000330010.12:c.658G>A	ENSP00000327363.8:p.Ala220Thr
ENST00000334785.11:c.850G>A	ENSP00000333938.7:p.Ala284Thr
ENST00000342754.5:c.549G>A
ENST00000401035.7:c.658G>A	ENSP00000383814.3:p.Ala220Thr
ENST00000440324.5:c.808G>A	ENSP00000411902.1:p.Ala270Thr
ENST00000464998.1:n.310G>A
NM_001172309.1:c.658G>A	NP_001165780.1:p.Ala220Thr
NM_144573.3:c.850G>A , LRG_442t1:c.850G>A	NP_653174.3:p.Ala284Thr
XM_005271322.2:c.850G>A	XP_005271379.1:p.Ala284Thr
XM_005271323.2:c.808G>A	XP_005271380.1:p.Ala270Thr
XM_005271324.3:c.658G>A	XP_005271381.1:p.Ala220Thr
XM_005271325.2:c.850G>A	XP_005271382.1:p.Ala284Thr
XM_005271326.2:c.616G>A	XP_005271383.1:p.Ala206Thr
XM_005271327.2:c.448-2438G>A	XP_005271384.1:n.448-2438G>A
XM_005271322.4:c.850G>A	XP_005271379.1:p.Ala284Thr
XM_005271323.4:c.808G>A	XP_005271380.1:p.Ala270Thr
XM_005271324.5:c.658G>A	XP_005271381.1:p.Ala220Thr
XM_005271325.4:c.850G>A	XP_005271382.1:p.Ala284Thr
XM_005271326.4:c.616G>A	XP_005271383.1:p.Ala206Thr
XM_005271327.4:c.448-2438G>A	XP_005271384.1:n.448-2438G>A
NM_001172309.2:c.658G>A	NP_001165780.1:p.Ala220Thr
NM_144573.4:c.850G>A MANE Select	NP_653174.3:p.Ala284Thr