Canonical Allele Identifier: CA2646301310

Gene: NEXN

Linked Data

• gnomAD v4: 1-77943076-TACTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943077_77943081del , CM000663.2:g.77943077_77943081del	GRCh38
NC_000001.10:g.78408762_78408766del , CM000663.1:g.78408762_78408766del	GRCh37
NC_000001.9:g.78181350_78181354del	NCBI36
NG_016625.1:g.59563_59567del , LRG_442:g.59563_59567del
NG_033243.2:g.41013_41017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*248_*252del MANE Select	ENSP00000333938.7:n.*248_*252del
ENST00000330010.12:c.*248_*252del	ENSP00000327363.8:n.*248_*252del
ENST00000334785.11:c.*248_*252del	ENSP00000333938.7:n.*248_*252del
ENST00000342754.5:c.1894_1898del
ENST00000480732.2:n.1850_1854del
NM_001172309.1:c.*248_*252del	NP_001165780.1:n.*248_*252del
NM_144573.3:c.*248_*252del , LRG_442t1:c.*248_*252del	NP_653174.3:n.*248_*252del
XM_005271322.2:c.*164_*168del	XP_005271379.1:n.*164_*168del
XM_005271323.2:c.*164_*168del	XP_005271380.1:n.*164_*168del
XM_005271324.3:c.*164_*168del	XP_005271381.1:n.*164_*168del
XM_005271325.2:c.*164_*168del	XP_005271382.1:n.*164_*168del
XM_005271326.2:c.*164_*168del	XP_005271383.1:n.*164_*168del
XM_005271327.2:c.*164_*168del	XP_005271384.1:n.*164_*168del
XM_005271322.4:c.*164_*168del	XP_005271379.1:n.*164_*168del
XM_005271323.4:c.*164_*168del	XP_005271380.1:n.*164_*168del
XM_005271324.5:c.*164_*168del	XP_005271381.1:n.*164_*168del
XM_005271325.4:c.*164_*168del	XP_005271382.1:n.*164_*168del
XM_005271326.4:c.*164_*168del	XP_005271383.1:n.*164_*168del
XM_005271327.4:c.*164_*168del	XP_005271384.1:n.*164_*168del
NM_001172309.2:c.*248_*252del	NP_001165780.1:n.*248_*252del
NM_144573.4:c.*248_*252del MANE Select	NP_653174.3:n.*248_*252del