Canonical Allele Identifier: CA418709509

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401702A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936017A>G , CM000663.2:g.77936017A>G	GRCh38
NC_000001.10:g.78401702A>G , CM000663.1:g.78401702A>G	GRCh37
NC_000001.9:g.78174290A>G	NCBI36
NG_016625.1:g.52503A>G , LRG_442:g.52503A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1446A>G MANE Select	ENSP00000333938.7:p.Lys482=
ENST00000330010.12:c.1254A>G	ENSP00000327363.8:p.Lys418=
ENST00000334785.11:c.1446A>G	ENSP00000333938.7:p.Lys482=
ENST00000342754.5:c.1145A>G
ENST00000480732.2:n.1020A>G
NM_001172309.1:c.1254A>G	NP_001165780.1:p.Lys418=
NM_144573.3:c.1446A>G , LRG_442t1:c.1446A>G	NP_653174.3:p.Lys482=
XM_005271322.2:c.1446A>G	XP_005271379.1:p.Lys482=
XM_005271323.2:c.1404A>G	XP_005271380.1:p.Lys468=
XM_005271324.3:c.1254A>G	XP_005271381.1:p.Lys418=
XM_005271325.2:c.1251+2538A>G	XP_005271382.1:n.1251+2538A>G
XM_005271326.2:c.1212A>G	XP_005271383.1:p.Lys404=
XM_005271327.2:c.1029A>G	XP_005271384.1:p.Lys343=
XM_005271322.4:c.1446A>G	XP_005271379.1:p.Lys482=
XM_005271323.4:c.1404A>G	XP_005271380.1:p.Lys468=
XM_005271324.5:c.1254A>G	XP_005271381.1:p.Lys418=
XM_005271325.4:c.1251+2538A>G	XP_005271382.1:n.1251+2538A>G
XM_005271326.4:c.1212A>G	XP_005271383.1:p.Lys404=
XM_005271327.4:c.1029A>G	XP_005271384.1:p.Lys343=
NM_001172309.2:c.1254A>G	NP_001165780.1:p.Lys418=
NM_144573.4:c.1446A>G MANE Select	NP_653174.3:p.Lys482=