Canonical Allele Identifier: CA2646275721

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942843-CTTTTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942846_77942850del , CM000663.2:g.77942846_77942850del	GRCh38
NC_000001.10:g.78408531_78408535del , CM000663.1:g.78408531_78408535del	GRCh37
NC_000001.9:g.78181119_78181123del	NCBI36
NG_016625.1:g.59332_59336del , LRG_442:g.59332_59336del
NG_033243.2:g.41246_41250del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*17_*21del MANE Select	ENSP00000333938.7:n.*17_*21del
ENST00000330010.12:c.*17_*21del	ENSP00000327363.8:n.*17_*21del
ENST00000334785.11:c.*17_*21del	ENSP00000333938.7:n.*17_*21del
ENST00000342754.5:c.1716+28_1716+32del
ENST00000480732.2:n.1619_1623del
NM_001172309.1:c.*17_*21del	NP_001165780.1:n.*17_*21del
NM_144573.3:c.*17_*21del , LRG_442t1:c.*17_*21del	NP_653174.3:n.*17_*21del
XM_005271322.2:c.2017+28_2017+32del	XP_005271379.1:n.2017+28_2017+32del
XM_005271323.2:c.1975+28_1975+32del	XP_005271380.1:n.1975+28_1975+32del
XM_005271324.3:c.1825+28_1825+32del	XP_005271381.1:n.1825+28_1825+32del
XM_005271325.2:c.1795+28_1795+32del	XP_005271382.1:n.1795+28_1795+32del
XM_005271326.2:c.1783+28_1783+32del	XP_005271383.1:n.1783+28_1783+32del
XM_005271327.2:c.1600+28_1600+32del	XP_005271384.1:n.1600+28_1600+32del
XM_005271322.4:c.2017+28_2017+32del	XP_005271379.1:n.2017+28_2017+32del
XM_005271323.4:c.1975+28_1975+32del	XP_005271380.1:n.1975+28_1975+32del
XM_005271324.5:c.1825+28_1825+32del	XP_005271381.1:n.1825+28_1825+32del
XM_005271325.4:c.1795+28_1795+32del	XP_005271382.1:n.1795+28_1795+32del
XM_005271326.4:c.1783+28_1783+32del	XP_005271383.1:n.1783+28_1783+32del
XM_005271327.4:c.1600+28_1600+32del	XP_005271384.1:n.1600+28_1600+32del
NM_001172309.2:c.*17_*21del	NP_001165780.1:n.*17_*21del
NM_144573.4:c.*17_*21del MANE Select	NP_653174.3:n.*17_*21del