Canonical Allele Identifier: CA340879345

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401683C>T (hg19) ; chr1:g.77935998C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935998C>T , CM000663.2:g.77935998C>T	GRCh38
NC_000001.10:g.78401683C>T , CM000663.1:g.78401683C>T	GRCh37
NC_000001.9:g.78174271C>T	NCBI36
NG_016625.1:g.52484C>T , LRG_442:g.52484C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1427C>T MANE Select	ENSP00000333938.7:p.Ala476Val
ENST00000330010.12:c.1235C>T	ENSP00000327363.8:p.Ala412Val
ENST00000334785.11:c.1427C>T	ENSP00000333938.7:p.Ala476Val
ENST00000342754.5:c.1126C>T
ENST00000480732.2:n.1001C>T
NM_001172309.1:c.1235C>T	NP_001165780.1:p.Ala412Val
NM_144573.3:c.1427C>T , LRG_442t1:c.1427C>T	NP_653174.3:p.Ala476Val
XM_005271322.2:c.1427C>T	XP_005271379.1:p.Ala476Val
XM_005271323.2:c.1385C>T	XP_005271380.1:p.Ala462Val
XM_005271324.3:c.1235C>T	XP_005271381.1:p.Ala412Val
XM_005271325.2:c.1251+2519C>T	XP_005271382.1:n.1251+2519C>T
XM_005271326.2:c.1193C>T	XP_005271383.1:p.Ala398Val
XM_005271327.2:c.1010C>T	XP_005271384.1:p.Ala337Val
XM_005271322.4:c.1427C>T	XP_005271379.1:p.Ala476Val
XM_005271323.4:c.1385C>T	XP_005271380.1:p.Ala462Val
XM_005271324.5:c.1235C>T	XP_005271381.1:p.Ala412Val
XM_005271325.4:c.1251+2519C>T	XP_005271382.1:n.1251+2519C>T
XM_005271326.4:c.1193C>T	XP_005271383.1:p.Ala398Val
XM_005271327.4:c.1010C>T	XP_005271384.1:p.Ala337Val
NM_001172309.2:c.1235C>T	NP_001165780.1:p.Ala412Val
NM_144573.4:c.1427C>T MANE Select	NP_653174.3:p.Ala476Val