Canonical Allele Identifier: CA340881058

Gene: NEXN

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1561G>C MANE Select	ENSP00000333938.7:p.Ala521Pro
ENST00000330010.12:c.1369G>C	ENSP00000327363.8:p.Ala457Pro
ENST00000334785.11:c.1561G>C	ENSP00000333938.7:p.Ala521Pro
ENST00000342754.5:c.1260G>C
ENST00000470735.1:n.400G>C
ENST00000480732.2:n.1135G>C
NM_001172309.1:c.1369G>C	NP_001165780.1:p.Ala457Pro
NM_144573.3:c.1561G>C , LRG_442t1:c.1561G>C	NP_653174.3:p.Ala521Pro
XM_005271322.2:c.1561G>C	XP_005271379.1:p.Ala521Pro
XM_005271323.2:c.1519G>C	XP_005271380.1:p.Ala507Pro
XM_005271324.3:c.1369G>C	XP_005271381.1:p.Ala457Pro
XM_005271325.2:c.1339G>C	XP_005271382.1:p.Ala447Pro
XM_005271326.2:c.1327G>C	XP_005271383.1:p.Ala443Pro
XM_005271327.2:c.1144G>C	XP_005271384.1:p.Ala382Pro
XM_005271322.4:c.1561G>C	XP_005271379.1:p.Ala521Pro
XM_005271323.4:c.1519G>C	XP_005271380.1:p.Ala507Pro
XM_005271324.5:c.1369G>C	XP_005271381.1:p.Ala457Pro
XM_005271325.4:c.1339G>C	XP_005271382.1:p.Ala447Pro
XM_005271326.4:c.1327G>C	XP_005271383.1:p.Ala443Pro
XM_005271327.4:c.1144G>C	XP_005271384.1:p.Ala382Pro
NM_001172309.2:c.1369G>C	NP_001165780.1:p.Ala457Pro
NM_144573.4:c.1561G>C MANE Select	NP_653174.3:p.Ala521Pro