Canonical Allele Identifier: CA418709484

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401684A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935999A>T , CM000663.2:g.77935999A>T	GRCh38
NC_000001.10:g.78401684A>T , CM000663.1:g.78401684A>T	GRCh37
NC_000001.9:g.78174272A>T	NCBI36
NG_016625.1:g.52485A>T , LRG_442:g.52485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1428A>T MANE Select	ENSP00000333938.7:p.Ala476=
ENST00000330010.12:c.1236A>T	ENSP00000327363.8:p.Ala412=
ENST00000334785.11:c.1428A>T	ENSP00000333938.7:p.Ala476=
ENST00000342754.5:c.1127A>T
ENST00000480732.2:n.1002A>T
NM_001172309.1:c.1236A>T	NP_001165780.1:p.Ala412=
NM_144573.3:c.1428A>T , LRG_442t1:c.1428A>T	NP_653174.3:p.Ala476=
XM_005271322.2:c.1428A>T	XP_005271379.1:p.Ala476=
XM_005271323.2:c.1386A>T	XP_005271380.1:p.Ala462=
XM_005271324.3:c.1236A>T	XP_005271381.1:p.Ala412=
XM_005271325.2:c.1251+2520A>T	XP_005271382.1:n.1251+2520A>T
XM_005271326.2:c.1194A>T	XP_005271383.1:p.Ala398=
XM_005271327.2:c.1011A>T	XP_005271384.1:p.Ala337=
XM_005271322.4:c.1428A>T	XP_005271379.1:p.Ala476=
XM_005271323.4:c.1386A>T	XP_005271380.1:p.Ala462=
XM_005271324.5:c.1236A>T	XP_005271381.1:p.Ala412=
XM_005271325.4:c.1251+2520A>T	XP_005271382.1:n.1251+2520A>T
XM_005271326.4:c.1194A>T	XP_005271383.1:p.Ala398=
XM_005271327.4:c.1011A>T	XP_005271384.1:p.Ala337=
NM_001172309.2:c.1236A>T	NP_001165780.1:p.Ala412=
NM_144573.4:c.1428A>T MANE Select	NP_653174.3:p.Ala476=