Canonical Allele Identifier: CA2646301314

Gene: NEXN

Linked Data

• gnomAD v4: 1-77943081-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943081C>A , CM000663.2:g.77943081C>A	GRCh38
NC_000001.10:g.78408766C>A , CM000663.1:g.78408766C>A	GRCh37
NC_000001.9:g.78181354C>A	NCBI36
NG_016625.1:g.59567C>A , LRG_442:g.59567C>A
NG_033243.2:g.41013G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*252C>A MANE Select	ENSP00000333938.7:n.*252C>A
ENST00000330010.12:c.*252C>A	ENSP00000327363.8:n.*252C>A
ENST00000334785.11:c.*252C>A	ENSP00000333938.7:n.*252C>A
ENST00000342754.5:c.1898C>A
ENST00000480732.2:n.1854C>A
NM_001172309.1:c.*252C>A	NP_001165780.1:n.*252C>A
NM_144573.3:c.*252C>A , LRG_442t1:c.*252C>A	NP_653174.3:n.*252C>A
XM_005271322.2:c.*168C>A	XP_005271379.1:n.*168C>A
XM_005271323.2:c.*168C>A	XP_005271380.1:n.*168C>A
XM_005271324.3:c.*168C>A	XP_005271381.1:n.*168C>A
XM_005271325.2:c.*168C>A	XP_005271382.1:n.*168C>A
XM_005271326.2:c.*168C>A	XP_005271383.1:n.*168C>A
XM_005271327.2:c.*168C>A	XP_005271384.1:n.*168C>A
XM_005271322.4:c.*168C>A	XP_005271379.1:n.*168C>A
XM_005271323.4:c.*168C>A	XP_005271380.1:n.*168C>A
XM_005271324.5:c.*168C>A	XP_005271381.1:n.*168C>A
XM_005271325.4:c.*168C>A	XP_005271382.1:n.*168C>A
XM_005271326.4:c.*168C>A	XP_005271383.1:n.*168C>A
XM_005271327.4:c.*168C>A	XP_005271384.1:n.*168C>A
NM_001172309.2:c.*252C>A	NP_001165780.1:n.*252C>A
NM_144573.4:c.*252C>A MANE Select	NP_653174.3:n.*252C>A