Canonical Allele Identifier: CA2646301289

Gene: NEXN

Linked Data

• gnomAD v4: 1-77943047-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943048_77943049del , CM000663.2:g.77943048_77943049del	GRCh38
NC_000001.10:g.78408733_78408734del , CM000663.1:g.78408733_78408734del	GRCh37
NC_000001.9:g.78181321_78181322del	NCBI36
NG_016625.1:g.59534_59535del , LRG_442:g.59534_59535del
NG_033243.2:g.41045_41046del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*219_*220del MANE Select	ENSP00000333938.7:n.*219_*220del
ENST00000330010.12:c.*219_*220del	ENSP00000327363.8:n.*219_*220del
ENST00000334785.11:c.*219_*220del	ENSP00000333938.7:n.*219_*220del
ENST00000342754.5:c.1865_1866del
ENST00000480732.2:n.1821_1822del
NM_001172309.1:c.*219_*220del	NP_001165780.1:n.*219_*220del
NM_144573.3:c.*219_*220del , LRG_442t1:c.*219_*220del	NP_653174.3:n.*219_*220del
XM_005271322.2:c.*135_*136del	XP_005271379.1:n.*135_*136del
XM_005271323.2:c.*135_*136del	XP_005271380.1:n.*135_*136del
XM_005271324.3:c.*135_*136del	XP_005271381.1:n.*135_*136del
XM_005271325.2:c.*135_*136del	XP_005271382.1:n.*135_*136del
XM_005271326.2:c.*135_*136del	XP_005271383.1:n.*135_*136del
XM_005271327.2:c.*135_*136del	XP_005271384.1:n.*135_*136del
XM_005271322.4:c.*135_*136del	XP_005271379.1:n.*135_*136del
XM_005271323.4:c.*135_*136del	XP_005271380.1:n.*135_*136del
XM_005271324.5:c.*135_*136del	XP_005271381.1:n.*135_*136del
XM_005271325.4:c.*135_*136del	XP_005271382.1:n.*135_*136del
XM_005271326.4:c.*135_*136del	XP_005271383.1:n.*135_*136del
XM_005271327.4:c.*135_*136del	XP_005271384.1:n.*135_*136del
NM_001172309.2:c.*219_*220del	NP_001165780.1:n.*219_*220del
NM_144573.4:c.*219_*220del MANE Select	NP_653174.3:n.*219_*220del