Canonical Allele Identifier: CA340879019

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401620T>A (hg19) ; chr1:g.77935935T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935935T>A , CM000663.2:g.77935935T>A	GRCh38
NC_000001.10:g.78401620T>A , CM000663.1:g.78401620T>A	GRCh37
NC_000001.9:g.78174208T>A	NCBI36
NG_016625.1:g.52421T>A , LRG_442:g.52421T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1364T>A MANE Select	ENSP00000333938.7:p.Ile455Asn
ENST00000330010.12:c.1172T>A	ENSP00000327363.8:p.Ile391Asn
ENST00000334785.11:c.1364T>A	ENSP00000333938.7:p.Ile455Asn
ENST00000342754.5:c.1063T>A
ENST00000464998.1:n.824T>A
ENST00000480732.2:n.938T>A
NM_001172309.1:c.1172T>A	NP_001165780.1:p.Ile391Asn
NM_144573.3:c.1364T>A , LRG_442t1:c.1364T>A	NP_653174.3:p.Ile455Asn
XM_005271322.2:c.1364T>A	XP_005271379.1:p.Ile455Asn
XM_005271323.2:c.1322T>A	XP_005271380.1:p.Ile441Asn
XM_005271324.3:c.1172T>A	XP_005271381.1:p.Ile391Asn
XM_005271325.2:c.1251+2456T>A	XP_005271382.1:n.1251+2456T>A
XM_005271326.2:c.1130T>A	XP_005271383.1:p.Ile377Asn
XM_005271327.2:c.947T>A	XP_005271384.1:p.Ile316Asn
XM_005271322.4:c.1364T>A	XP_005271379.1:p.Ile455Asn
XM_005271323.4:c.1322T>A	XP_005271380.1:p.Ile441Asn
XM_005271324.5:c.1172T>A	XP_005271381.1:p.Ile391Asn
XM_005271325.4:c.1251+2456T>A	XP_005271382.1:n.1251+2456T>A
XM_005271326.4:c.1130T>A	XP_005271383.1:p.Ile377Asn
XM_005271327.4:c.947T>A	XP_005271384.1:p.Ile316Asn
NM_001172309.2:c.1172T>A	NP_001165780.1:p.Ile391Asn
NM_144573.4:c.1364T>A MANE Select	NP_653174.3:p.Ile455Asn