Canonical Allele Identifier: CA1177626245

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942878_77942893delinsCTTTTCTTCTTCTCTT , CM000663.2:g.77942878_77942893delinsCTTTTCTTCTTCTCTT	GRCh38
NC_000001.10:g.78408563_78408578delinsCTTTTCTTCTTCTCTT , CM000663.1:g.78408563_78408578delinsCTTTTCTTCTTCTCTT	GRCh37
NC_000001.9:g.78181151_78181166delinsCTTTTCTTCTTCTCTT	NCBI36
NG_016625.1:g.59364_59379delinsCTTTTCTTCTTCTCTT , LRG_442:g.59364_59379delinsCTTTTCTTCTTCTCTT
NG_033243.2:g.41201_41216delinsAAGAGAAGAAGAAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*49_*64delinsCTTTTCTTCTTCTCTT MANE Select	ENSP00000333938.7:n.*49_*64delinsCTTTTCTTCTTCTCTT
ENST00000330010.12:c.*49_*64delinsCTTTTCTTCTTCTCTT	ENSP00000327363.8:n.*49_*64delinsCTTTTCTTCTTCTCTT
ENST00000334785.11:c.*49_*64delinsCTTTTCTTCTTCTCTT	ENSP00000333938.7:n.*49_*64delinsCTTTTCTTCTTCTCTT
ENST00000342754.5:c.1717-22_1717-7delinsCTTTTCTTCTTCTCTT
ENST00000480732.2:n.1651_1666delinsCTTTTCTTCTTCTCTT
NM_001172309.1:c.*49_*64delinsCTTTTCTTCTTCTCTT	NP_001165780.1:n.*49_*64delinsCTTTTCTTCTTCTCTT
NM_144573.3:c.*49_*64delinsCTTTTCTTCTTCTCTT , LRG_442t1:c.*49_*64delinsCTTTTCTTCTTCTCTT	NP_653174.3:n.*49_*64delinsCTTTTCTTCTTCTCTT
XM_005271322.2:c.2018-22_2018-7delinsCTTTTCTTCTTCTCTT	XP_005271379.1:n.2018-22_2018-7delinsCTTTTCTTCTTCTCTT
XM_005271323.2:c.1976-22_1976-7delinsCTTTTCTTCTTCTCTT	XP_005271380.1:n.1976-22_1976-7delinsCTTTTCTTCTTCTCTT
XM_005271324.3:c.1826-22_1826-7delinsCTTTTCTTCTTCTCTT	XP_005271381.1:n.1826-22_1826-7delinsCTTTTCTTCTTCTCTT
XM_005271325.2:c.1796-22_1796-7delinsCTTTTCTTCTTCTCTT	XP_005271382.1:n.1796-22_1796-7delinsCTTTTCTTCTTCTCTT
XM_005271326.2:c.1784-22_1784-7delinsCTTTTCTTCTTCTCTT	XP_005271383.1:n.1784-22_1784-7delinsCTTTTCTTCTTCTCTT
XM_005271327.2:c.1601-22_1601-7delinsCTTTTCTTCTTCTCTT	XP_005271384.1:n.1601-22_1601-7delinsCTTTTCTTCTTCTCTT
XM_005271322.4:c.2018-22_2018-7delinsCTTTTCTTCTTCTCTT	XP_005271379.1:n.2018-22_2018-7delinsCTTTTCTTCTTCTCTT
XM_005271323.4:c.1976-22_1976-7delinsCTTTTCTTCTTCTCTT	XP_005271380.1:n.1976-22_1976-7delinsCTTTTCTTCTTCTCTT
XM_005271324.5:c.1826-22_1826-7delinsCTTTTCTTCTTCTCTT	XP_005271381.1:n.1826-22_1826-7delinsCTTTTCTTCTTCTCTT
XM_005271325.4:c.1796-22_1796-7delinsCTTTTCTTCTTCTCTT	XP_005271382.1:n.1796-22_1796-7delinsCTTTTCTTCTTCTCTT
XM_005271326.4:c.1784-22_1784-7delinsCTTTTCTTCTTCTCTT	XP_005271383.1:n.1784-22_1784-7delinsCTTTTCTTCTTCTCTT
XM_005271327.4:c.1601-22_1601-7delinsCTTTTCTTCTTCTCTT	XP_005271384.1:n.1601-22_1601-7delinsCTTTTCTTCTTCTCTT
NM_001172309.2:c.*49_*64delinsCTTTTCTTCTTCTCTT	NP_001165780.1:n.*49_*64delinsCTTTTCTTCTTCTCTT
NM_144573.4:c.*49_*64delinsCTTTTCTTCTTCTCTT MANE Select	NP_653174.3:n.*49_*64delinsCTTTTCTTCTTCTCTT