Canonical Allele Identifier: CA340881064

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407795G>T (hg19) ; chr1:g.77942110G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942110G>T , CM000663.2:g.77942110G>T	GRCh38
NC_000001.10:g.78407795G>T , CM000663.1:g.78407795G>T	GRCh37
NC_000001.9:g.78180383G>T	NCBI36
NG_016625.1:g.58596G>T , LRG_442:g.58596G>T
NG_033243.2:g.41984C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1561G>T MANE Select	ENSP00000333938.7:p.Ala521Ser
ENST00000330010.12:c.1369G>T	ENSP00000327363.8:p.Ala457Ser
ENST00000334785.11:c.1561G>T	ENSP00000333938.7:p.Ala521Ser
ENST00000342754.5:c.1260G>T
ENST00000470735.1:n.400G>T
ENST00000480732.2:n.1135G>T
NM_001172309.1:c.1369G>T	NP_001165780.1:p.Ala457Ser
NM_144573.3:c.1561G>T , LRG_442t1:c.1561G>T	NP_653174.3:p.Ala521Ser
XM_005271322.2:c.1561G>T	XP_005271379.1:p.Ala521Ser
XM_005271323.2:c.1519G>T	XP_005271380.1:p.Ala507Ser
XM_005271324.3:c.1369G>T	XP_005271381.1:p.Ala457Ser
XM_005271325.2:c.1339G>T	XP_005271382.1:p.Ala447Ser
XM_005271326.2:c.1327G>T	XP_005271383.1:p.Ala443Ser
XM_005271327.2:c.1144G>T	XP_005271384.1:p.Ala382Ser
XM_005271322.4:c.1561G>T	XP_005271379.1:p.Ala521Ser
XM_005271323.4:c.1519G>T	XP_005271380.1:p.Ala507Ser
XM_005271324.5:c.1369G>T	XP_005271381.1:p.Ala457Ser
XM_005271325.4:c.1339G>T	XP_005271382.1:p.Ala447Ser
XM_005271326.4:c.1327G>T	XP_005271383.1:p.Ala443Ser
XM_005271327.4:c.1144G>T	XP_005271384.1:p.Ala382Ser
NM_001172309.2:c.1369G>T	NP_001165780.1:p.Ala457Ser
NM_144573.4:c.1561G>T MANE Select	NP_653174.3:p.Ala521Ser