Canonical Allele Identifier: CA340878513

Gene: NEXN

Linked Data

• gnomAD v4: 1-77935878-A-T
• MyVariant Identifiers: chr1:g.78401563A>T (hg19) ; chr1:g.77935878A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935878A>T , CM000663.2:g.77935878A>T	GRCh38
NC_000001.10:g.78401563A>T , CM000663.1:g.78401563A>T	GRCh37
NC_000001.9:g.78174151A>T	NCBI36
NG_016625.1:g.52364A>T , LRG_442:g.52364A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1307A>T MANE Select	ENSP00000333938.7:p.Lys436Ile
ENST00000330010.12:c.1115A>T	ENSP00000327363.8:p.Lys372Ile
ENST00000334785.11:c.1307A>T	ENSP00000333938.7:p.Lys436Ile
ENST00000342754.5:c.1006A>T
ENST00000440324.5:c.1265A>T	ENSP00000411902.1:p.Lys422Ile
ENST00000464998.1:n.767A>T
ENST00000480732.2:n.881A>T
NM_001172309.1:c.1115A>T	NP_001165780.1:p.Lys372Ile
NM_144573.3:c.1307A>T , LRG_442t1:c.1307A>T	NP_653174.3:p.Lys436Ile
XM_005271322.2:c.1307A>T	XP_005271379.1:p.Lys436Ile
XM_005271323.2:c.1265A>T	XP_005271380.1:p.Lys422Ile
XM_005271324.3:c.1115A>T	XP_005271381.1:p.Lys372Ile
XM_005271325.2:c.1251+2399A>T	XP_005271382.1:n.1251+2399A>T
XM_005271326.2:c.1073A>T	XP_005271383.1:p.Lys358Ile
XM_005271327.2:c.890A>T	XP_005271384.1:p.Lys297Ile
XM_005271322.4:c.1307A>T	XP_005271379.1:p.Lys436Ile
XM_005271323.4:c.1265A>T	XP_005271380.1:p.Lys422Ile
XM_005271324.5:c.1115A>T	XP_005271381.1:p.Lys372Ile
XM_005271325.4:c.1251+2399A>T	XP_005271382.1:n.1251+2399A>T
XM_005271326.4:c.1073A>T	XP_005271383.1:p.Lys358Ile
XM_005271327.4:c.890A>T	XP_005271384.1:p.Lys297Ile
NM_001172309.2:c.1115A>T	NP_001165780.1:p.Lys372Ile
NM_144573.4:c.1307A>T MANE Select	NP_653174.3:p.Lys436Ile