Canonical Allele Identifier: CA340878758

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401590C>G (hg19) ; chr1:g.77935905C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935905C>G , CM000663.2:g.77935905C>G	GRCh38
NC_000001.10:g.78401590C>G , CM000663.1:g.78401590C>G	GRCh37
NC_000001.9:g.78174178C>G	NCBI36
NG_016625.1:g.52391C>G , LRG_442:g.52391C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1334C>G MANE Select	ENSP00000333938.7:p.Ala445Gly
ENST00000330010.12:c.1142C>G	ENSP00000327363.8:p.Ala381Gly
ENST00000334785.11:c.1334C>G	ENSP00000333938.7:p.Ala445Gly
ENST00000342754.5:c.1033C>G
ENST00000440324.5:c.1292C>G	ENSP00000411902.1:p.Ala431Gly
ENST00000464998.1:n.794C>G
ENST00000480732.2:n.908C>G
NM_001172309.1:c.1142C>G	NP_001165780.1:p.Ala381Gly
NM_144573.3:c.1334C>G , LRG_442t1:c.1334C>G	NP_653174.3:p.Ala445Gly
XM_005271322.2:c.1334C>G	XP_005271379.1:p.Ala445Gly
XM_005271323.2:c.1292C>G	XP_005271380.1:p.Ala431Gly
XM_005271324.3:c.1142C>G	XP_005271381.1:p.Ala381Gly
XM_005271325.2:c.1251+2426C>G	XP_005271382.1:n.1251+2426C>G
XM_005271326.2:c.1100C>G	XP_005271383.1:p.Ala367Gly
XM_005271327.2:c.917C>G	XP_005271384.1:p.Ala306Gly
XM_005271322.4:c.1334C>G	XP_005271379.1:p.Ala445Gly
XM_005271323.4:c.1292C>G	XP_005271380.1:p.Ala431Gly
XM_005271324.5:c.1142C>G	XP_005271381.1:p.Ala381Gly
XM_005271325.4:c.1251+2426C>G	XP_005271382.1:n.1251+2426C>G
XM_005271326.4:c.1100C>G	XP_005271383.1:p.Ala367Gly
XM_005271327.4:c.917C>G	XP_005271384.1:p.Ala306Gly
NM_001172309.2:c.1142C>G	NP_001165780.1:p.Ala381Gly
NM_144573.4:c.1334C>G MANE Select	NP_653174.3:p.Ala445Gly