Canonical Allele Identifier: CA2646301331

Gene: NEXN

Linked Data

• gnomAD v4: 1-77943109-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943109C>T , CM000663.2:g.77943109C>T	GRCh38
NC_000001.10:g.78408794C>T , CM000663.1:g.78408794C>T	GRCh37
NC_000001.9:g.78181382C>T	NCBI36
NG_016625.1:g.59595C>T , LRG_442:g.59595C>T
NG_033243.2:g.40985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*280C>T MANE Select	ENSP00000333938.7:n.*280C>T
ENST00000330010.12:c.*280C>T	ENSP00000327363.8:n.*280C>T
ENST00000334785.11:c.*280C>T	ENSP00000333938.7:n.*280C>T
ENST00000342754.5:c.1926C>T
ENST00000480732.2:n.1882C>T
NM_001172309.1:c.*280C>T	NP_001165780.1:n.*280C>T
NM_144573.3:c.*280C>T , LRG_442t1:c.*280C>T	NP_653174.3:n.*280C>T
XM_005271322.2:c.*196C>T	XP_005271379.1:n.*196C>T
XM_005271323.2:c.*196C>T	XP_005271380.1:n.*196C>T
XM_005271324.3:c.*196C>T	XP_005271381.1:n.*196C>T
XM_005271325.2:c.*196C>T	XP_005271382.1:n.*196C>T
XM_005271326.2:c.*196C>T	XP_005271383.1:n.*196C>T
XM_005271327.2:c.*196C>T	XP_005271384.1:n.*196C>T
XM_005271322.4:c.*196C>T	XP_005271379.1:n.*196C>T
XM_005271323.4:c.*196C>T	XP_005271380.1:n.*196C>T
XM_005271324.5:c.*196C>T	XP_005271381.1:n.*196C>T
XM_005271325.4:c.*196C>T	XP_005271382.1:n.*196C>T
XM_005271326.4:c.*196C>T	XP_005271383.1:n.*196C>T
XM_005271327.4:c.*196C>T	XP_005271384.1:n.*196C>T
NM_001172309.2:c.*280C>T	NP_001165780.1:n.*280C>T
NM_144573.4:c.*280C>T MANE Select	NP_653174.3:n.*280C>T