Canonical Allele Identifier: CA2646301244

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942979-GTGGCGGGGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942980_77942989del , CM000663.2:g.77942980_77942989del	GRCh38
NC_000001.10:g.78408665_78408674del , CM000663.1:g.78408665_78408674del	GRCh37
NC_000001.9:g.78181253_78181262del	NCBI36
NG_016625.1:g.59466_59475del , LRG_442:g.59466_59475del
NG_033243.2:g.41105_41114del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*151_*160del MANE Select	ENSP00000333938.7:n.*151_*160del
ENST00000330010.12:c.*151_*160del	ENSP00000327363.8:n.*151_*160del
ENST00000334785.11:c.*151_*160del	ENSP00000333938.7:n.*151_*160del
ENST00000342754.5:c.1797_1806del
ENST00000480732.2:n.1753_1762del
NM_001172309.1:c.*151_*160del	NP_001165780.1:n.*151_*160del
NM_144573.3:c.*151_*160del , LRG_442t1:c.*151_*160del	NP_653174.3:n.*151_*160del
XM_005271322.2:c.*67_*76del	XP_005271379.1:n.*67_*76del
XM_005271323.2:c.*67_*76del	XP_005271380.1:n.*67_*76del
XM_005271324.3:c.*67_*76del	XP_005271381.1:n.*67_*76del
XM_005271325.2:c.*67_*76del	XP_005271382.1:n.*67_*76del
XM_005271326.2:c.*67_*76del	XP_005271383.1:n.*67_*76del
XM_005271327.2:c.*67_*76del	XP_005271384.1:n.*67_*76del
XM_005271322.4:c.*67_*76del	XP_005271379.1:n.*67_*76del
XM_005271323.4:c.*67_*76del	XP_005271380.1:n.*67_*76del
XM_005271324.5:c.*67_*76del	XP_005271381.1:n.*67_*76del
XM_005271325.4:c.*67_*76del	XP_005271382.1:n.*67_*76del
XM_005271326.4:c.*67_*76del	XP_005271383.1:n.*67_*76del
XM_005271327.4:c.*67_*76del	XP_005271384.1:n.*67_*76del
NM_001172309.2:c.*151_*160del	NP_001165780.1:n.*151_*160del
NM_144573.4:c.*151_*160del MANE Select	NP_653174.3:n.*151_*160del