Canonical Allele Identifier: CA739060023

Gene: NEXN

Linked Data

• dbSNP Id: rs1272161432
• gnomAD v4: 1-77942910-C-T
• MyVariant Identifiers: chr1:g.78408595C>T (hg19) ; chr1:g.77942910C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942910C>T , CM000663.2:g.77942910C>T	GRCh38
NC_000001.10:g.78408595C>T , CM000663.1:g.78408595C>T	GRCh37
NC_000001.9:g.78181183C>T	NCBI36
NG_016625.1:g.59396C>T , LRG_442:g.59396C>T
NG_033243.2:g.41184G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*81C>T MANE Select	ENSP00000333938.7:n.*81C>T
ENST00000330010.12:c.*81C>T	ENSP00000327363.8:n.*81C>T
ENST00000334785.11:c.*81C>T	ENSP00000333938.7:n.*81C>T
ENST00000342754.5:c.1727C>T
ENST00000480732.2:n.1683C>T
NM_001172309.1:c.*81C>T	NP_001165780.1:n.*81C>T
NM_144573.3:c.*81C>T , LRG_442t1:c.*81C>T	NP_653174.3:n.*81C>T
XM_005271322.2:c.2028C>T	XP_005271379.1:p.Tyr676=
XM_005271323.2:c.1986C>T	XP_005271380.1:p.Tyr662=
XM_005271324.3:c.1836C>T	XP_005271381.1:p.Tyr612=
XM_005271325.2:c.1806C>T	XP_005271382.1:p.Tyr602=
XM_005271326.2:c.1794C>T	XP_005271383.1:p.Tyr598=
XM_005271327.2:c.1611C>T	XP_005271384.1:p.Tyr537=
XM_005271322.4:c.2028C>T	XP_005271379.1:p.Tyr676=
XM_005271323.4:c.1986C>T	XP_005271380.1:p.Tyr662=
XM_005271324.5:c.1836C>T	XP_005271381.1:p.Tyr612=
XM_005271325.4:c.1806C>T	XP_005271382.1:p.Tyr602=
XM_005271326.4:c.1794C>T	XP_005271383.1:p.Tyr598=
XM_005271327.4:c.1611C>T	XP_005271384.1:p.Tyr537=
NM_001172309.2:c.*81C>T	NP_001165780.1:n.*81C>T
NM_144573.4:c.*81C>T MANE Select	NP_653174.3:n.*81C>T