Canonical Allele Identifier: CA2646275714

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942835-CTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942837_77942840del , CM000663.2:g.77942837_77942840del	GRCh38
NC_000001.10:g.78408522_78408525del , CM000663.1:g.78408522_78408525del	GRCh37
NC_000001.9:g.78181110_78181113del	NCBI36
NG_016625.1:g.59323_59326del , LRG_442:g.59323_59326del
NG_033243.2:g.41255_41258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*8_*11del MANE Select	ENSP00000333938.7:n.*8_*11del
ENST00000330010.12:c.*8_*11del	ENSP00000327363.8:n.*8_*11del
ENST00000334785.11:c.*8_*11del	ENSP00000333938.7:n.*8_*11del
ENST00000342754.5:c.1716+19_1716+22del
ENST00000480732.2:n.1610_1613del
NM_001172309.1:c.*8_*11del	NP_001165780.1:n.*8_*11del
NM_144573.3:c.*8_*11del , LRG_442t1:c.*8_*11del	NP_653174.3:n.*8_*11del
XM_005271322.2:c.2017+19_2017+22del	XP_005271379.1:n.2017+19_2017+22del
XM_005271323.2:c.1975+19_1975+22del	XP_005271380.1:n.1975+19_1975+22del
XM_005271324.3:c.1825+19_1825+22del	XP_005271381.1:n.1825+19_1825+22del
XM_005271325.2:c.1795+19_1795+22del	XP_005271382.1:n.1795+19_1795+22del
XM_005271326.2:c.1783+19_1783+22del	XP_005271383.1:n.1783+19_1783+22del
XM_005271327.2:c.1600+19_1600+22del	XP_005271384.1:n.1600+19_1600+22del
XM_005271322.4:c.2017+19_2017+22del	XP_005271379.1:n.2017+19_2017+22del
XM_005271323.4:c.1975+19_1975+22del	XP_005271380.1:n.1975+19_1975+22del
XM_005271324.5:c.1825+19_1825+22del	XP_005271381.1:n.1825+19_1825+22del
XM_005271325.4:c.1795+19_1795+22del	XP_005271382.1:n.1795+19_1795+22del
XM_005271326.4:c.1783+19_1783+22del	XP_005271383.1:n.1783+19_1783+22del
XM_005271327.4:c.1600+19_1600+22del	XP_005271384.1:n.1600+19_1600+22del
NM_001172309.2:c.*8_*11del	NP_001165780.1:n.*8_*11del
NM_144573.4:c.*8_*11del MANE Select	NP_653174.3:n.*8_*11del