Canonical Allele Identifier: CA739060030

Gene: NEXN

Linked Data

• dbSNP Id: rs1400773161
• gnomAD v3: 1-77942914-C-T
• gnomAD v4: 1-77942914-C-T
• MyVariant Identifiers: chr1:g.78408599C>T (hg19) ; chr1:g.77942914C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942914C>T , CM000663.2:g.77942914C>T	GRCh38
NC_000001.10:g.78408599C>T , CM000663.1:g.78408599C>T	GRCh37
NC_000001.9:g.78181187C>T	NCBI36
NG_016625.1:g.59400C>T , LRG_442:g.59400C>T
NG_033243.2:g.41180G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*85C>T MANE Select	ENSP00000333938.7:n.*85C>T
ENST00000330010.12:c.*85C>T	ENSP00000327363.8:n.*85C>T
ENST00000334785.11:c.*85C>T	ENSP00000333938.7:n.*85C>T
ENST00000342754.5:c.1731C>T
ENST00000480732.2:n.1687C>T
NM_001172309.1:c.*85C>T	NP_001165780.1:n.*85C>T
NM_144573.3:c.*85C>T , LRG_442t1:c.*85C>T	NP_653174.3:n.*85C>T
XM_005271322.2:c.*1C>T	XP_005271379.1:n.*1C>T
XM_005271323.2:c.*1C>T	XP_005271380.1:n.*1C>T
XM_005271324.3:c.*1C>T	XP_005271381.1:n.*1C>T
XM_005271325.2:c.*1C>T	XP_005271382.1:n.*1C>T
XM_005271326.2:c.*1C>T	XP_005271383.1:n.*1C>T
XM_005271327.2:c.*1C>T	XP_005271384.1:n.*1C>T
XM_005271322.4:c.*1C>T	XP_005271379.1:n.*1C>T
XM_005271323.4:c.*1C>T	XP_005271380.1:n.*1C>T
XM_005271324.5:c.*1C>T	XP_005271381.1:n.*1C>T
XM_005271325.4:c.*1C>T	XP_005271382.1:n.*1C>T
XM_005271326.4:c.*1C>T	XP_005271383.1:n.*1C>T
XM_005271327.4:c.*1C>T	XP_005271384.1:n.*1C>T
NM_001172309.2:c.*85C>T	NP_001165780.1:n.*85C>T
NM_144573.4:c.*85C>T MANE Select	NP_653174.3:n.*85C>T