Canonical Allele Identifier: CA2646275806

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942907-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942907C>A , CM000663.2:g.77942907C>A	GRCh38
NC_000001.10:g.78408592C>A , CM000663.1:g.78408592C>A	GRCh37
NC_000001.9:g.78181180C>A	NCBI36
NG_016625.1:g.59393C>A , LRG_442:g.59393C>A
NG_033243.2:g.41187G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*78C>A MANE Select	ENSP00000333938.7:n.*78C>A
ENST00000330010.12:c.*78C>A	ENSP00000327363.8:n.*78C>A
ENST00000334785.11:c.*78C>A	ENSP00000333938.7:n.*78C>A
ENST00000342754.5:c.1724C>A
ENST00000480732.2:n.1680C>A
NM_001172309.1:c.*78C>A	NP_001165780.1:n.*78C>A
NM_144573.3:c.*78C>A , LRG_442t1:c.*78C>A	NP_653174.3:n.*78C>A
XM_005271322.2:c.2025C>A	XP_005271379.1:p.Asp675Glu
XM_005271323.2:c.1983C>A	XP_005271380.1:p.Asp661Glu
XM_005271324.3:c.1833C>A	XP_005271381.1:p.Asp611Glu
XM_005271325.2:c.1803C>A	XP_005271382.1:p.Asp601Glu
XM_005271326.2:c.1791C>A	XP_005271383.1:p.Asp597Glu
XM_005271327.2:c.1608C>A	XP_005271384.1:p.Asp536Glu
XM_005271322.4:c.2025C>A	XP_005271379.1:p.Asp675Glu
XM_005271323.4:c.1983C>A	XP_005271380.1:p.Asp661Glu
XM_005271324.5:c.1833C>A	XP_005271381.1:p.Asp611Glu
XM_005271325.4:c.1803C>A	XP_005271382.1:p.Asp601Glu
XM_005271326.4:c.1791C>A	XP_005271383.1:p.Asp597Glu
XM_005271327.4:c.1608C>A	XP_005271384.1:p.Asp536Glu
NM_001172309.2:c.*78C>A	NP_001165780.1:n.*78C>A
NM_144573.4:c.*78C>A MANE Select	NP_653174.3:n.*78C>A