Canonical Allele Identifier: CA1177626185

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942853_77942858delinsATTAAT , CM000663.2:g.77942853_77942858delinsATTAAT	GRCh38
NC_000001.10:g.78408538_78408543delinsATTAAT , CM000663.1:g.78408538_78408543delinsATTAAT	GRCh37
NC_000001.9:g.78181126_78181131delinsATTAAT	NCBI36
NG_016625.1:g.59339_59344delinsATTAAT , LRG_442:g.59339_59344delinsATTAAT
NG_033243.2:g.41236_41241delinsATTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*24_*29delinsATTAAT MANE Select	ENSP00000333938.7:n.*24_*29delinsATTAAT
ENST00000330010.12:c.*24_*29delinsATTAAT	ENSP00000327363.8:n.*24_*29delinsATTAAT
ENST00000334785.11:c.*24_*29delinsATTAAT	ENSP00000333938.7:n.*24_*29delinsATTAAT
ENST00000342754.5:c.1716+35_1716+40delinsATTAAT
ENST00000480732.2:n.1626_1631delinsATTAAT
NM_001172309.1:c.*24_*29delinsATTAAT	NP_001165780.1:n.*24_*29delinsATTAAT
NM_144573.3:c.*24_*29delinsATTAAT , LRG_442t1:c.*24_*29delinsATTAAT	NP_653174.3:n.*24_*29delinsATTAAT
XM_005271322.2:c.2017+35_2017+40delinsATTAAT	XP_005271379.1:n.2017+35_2017+40delinsATTAAT
XM_005271323.2:c.1975+35_1975+40delinsATTAAT	XP_005271380.1:n.1975+35_1975+40delinsATTAAT
XM_005271324.3:c.1825+35_1825+40delinsATTAAT	XP_005271381.1:n.1825+35_1825+40delinsATTAAT
XM_005271325.2:c.1795+35_1795+40delinsATTAAT	XP_005271382.1:n.1795+35_1795+40delinsATTAAT
XM_005271326.2:c.1783+35_1783+40delinsATTAAT	XP_005271383.1:n.1783+35_1783+40delinsATTAAT
XM_005271327.2:c.1600+35_1600+40delinsATTAAT	XP_005271384.1:n.1600+35_1600+40delinsATTAAT
XM_005271322.4:c.2017+35_2017+40delinsATTAAT	XP_005271379.1:n.2017+35_2017+40delinsATTAAT
XM_005271323.4:c.1975+35_1975+40delinsATTAAT	XP_005271380.1:n.1975+35_1975+40delinsATTAAT
XM_005271324.5:c.1825+35_1825+40delinsATTAAT	XP_005271381.1:n.1825+35_1825+40delinsATTAAT
XM_005271325.4:c.1795+35_1795+40delinsATTAAT	XP_005271382.1:n.1795+35_1795+40delinsATTAAT
XM_005271326.4:c.1783+35_1783+40delinsATTAAT	XP_005271383.1:n.1783+35_1783+40delinsATTAAT
XM_005271327.4:c.1600+35_1600+40delinsATTAAT	XP_005271384.1:n.1600+35_1600+40delinsATTAAT
NM_001172309.2:c.*24_*29delinsATTAAT	NP_001165780.1:n.*24_*29delinsATTAAT
NM_144573.4:c.*24_*29delinsATTAAT MANE Select	NP_653174.3:n.*24_*29delinsATTAAT