Canonical Allele Identifier: CA340874582

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78392552C>A (hg19) ; chr1:g.77926867C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77926867C>A , CM000663.2:g.77926867C>A	GRCh38
NC_000001.10:g.78392552C>A , CM000663.1:g.78392552C>A	GRCh37
NC_000001.9:g.78165140C>A	NCBI36
NG_016625.1:g.43353C>A , LRG_442:g.43353C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.839C>A MANE Select	ENSP00000333938.7:p.Ala280Asp
ENST00000330010.12:c.647C>A	ENSP00000327363.8:p.Ala216Asp
ENST00000334785.11:c.839C>A	ENSP00000333938.7:p.Ala280Asp
ENST00000342754.5:c.538C>A
ENST00000401035.7:c.647C>A	ENSP00000383814.3:p.Ala216Asp
ENST00000440324.5:c.797C>A	ENSP00000411902.1:p.Ala266Asp
ENST00000464998.1:n.299C>A
NM_001172309.1:c.647C>A	NP_001165780.1:p.Ala216Asp
NM_144573.3:c.839C>A , LRG_442t1:c.839C>A	NP_653174.3:p.Ala280Asp
XM_005271322.2:c.839C>A	XP_005271379.1:p.Ala280Asp
XM_005271323.2:c.797C>A	XP_005271380.1:p.Ala266Asp
XM_005271324.3:c.647C>A	XP_005271381.1:p.Ala216Asp
XM_005271325.2:c.839C>A	XP_005271382.1:p.Ala280Asp
XM_005271326.2:c.605C>A	XP_005271383.1:p.Ala202Asp
XM_005271327.2:c.448-2449C>A	XP_005271384.1:n.448-2449C>A
XM_005271322.4:c.839C>A	XP_005271379.1:p.Ala280Asp
XM_005271323.4:c.797C>A	XP_005271380.1:p.Ala266Asp
XM_005271324.5:c.647C>A	XP_005271381.1:p.Ala216Asp
XM_005271325.4:c.839C>A	XP_005271382.1:p.Ala280Asp
XM_005271326.4:c.605C>A	XP_005271383.1:p.Ala202Asp
XM_005271327.4:c.448-2449C>A	XP_005271384.1:n.448-2449C>A
NM_001172309.2:c.647C>A	NP_001165780.1:p.Ala216Asp
NM_144573.4:c.839C>A MANE Select	NP_653174.3:p.Ala280Asp