Canonical Allele Identifier: CA340881055

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78407794G>T (hg19) ; chr1:g.77942109G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942109G>T , CM000663.2:g.77942109G>T	GRCh38
NC_000001.10:g.78407794G>T , CM000663.1:g.78407794G>T	GRCh37
NC_000001.9:g.78180382G>T	NCBI36
NG_016625.1:g.58595G>T , LRG_442:g.58595G>T
NG_033243.2:g.41985C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1560G>T MANE Select	ENSP00000333938.7:p.Met520Ile
ENST00000330010.12:c.1368G>T	ENSP00000327363.8:p.Met456Ile
ENST00000334785.11:c.1560G>T	ENSP00000333938.7:p.Met520Ile
ENST00000342754.5:c.1259G>T
ENST00000470735.1:n.399G>T
ENST00000480732.2:n.1134G>T
NM_001172309.1:c.1368G>T	NP_001165780.1:p.Met456Ile
NM_144573.3:c.1560G>T , LRG_442t1:c.1560G>T	NP_653174.3:p.Met520Ile
XM_005271322.2:c.1560G>T	XP_005271379.1:p.Met520Ile
XM_005271323.2:c.1518G>T	XP_005271380.1:p.Met506Ile
XM_005271324.3:c.1368G>T	XP_005271381.1:p.Met456Ile
XM_005271325.2:c.1338G>T	XP_005271382.1:p.Met446Ile
XM_005271326.2:c.1326G>T	XP_005271383.1:p.Met442Ile
XM_005271327.2:c.1143G>T	XP_005271384.1:p.Met381Ile
XM_005271322.4:c.1560G>T	XP_005271379.1:p.Met520Ile
XM_005271323.4:c.1518G>T	XP_005271380.1:p.Met506Ile
XM_005271324.5:c.1368G>T	XP_005271381.1:p.Met456Ile
XM_005271325.4:c.1338G>T	XP_005271382.1:p.Met446Ile
XM_005271326.4:c.1326G>T	XP_005271383.1:p.Met442Ile
XM_005271327.4:c.1143G>T	XP_005271384.1:p.Met381Ile
NM_001172309.2:c.1368G>T	NP_001165780.1:p.Met456Ile
NM_144573.4:c.1560G>T MANE Select	NP_653174.3:p.Met520Ile