Canonical Allele Identifier: CA1177626251

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942880_77942883delinsTTTC , CM000663.2:g.77942880_77942883delinsTTTC	GRCh38
NC_000001.10:g.78408565_78408568delinsTTTC , CM000663.1:g.78408565_78408568delinsTTTC	GRCh37
NC_000001.9:g.78181153_78181156delinsTTTC	NCBI36
NG_016625.1:g.59366_59369delinsTTTC , LRG_442:g.59366_59369delinsTTTC
NG_033243.2:g.41211_41214delinsGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*51_*54delinsTTTC MANE Select	ENSP00000333938.7:n.*51_*54delinsTTTC
ENST00000330010.12:c.*51_*54delinsTTTC	ENSP00000327363.8:n.*51_*54delinsTTTC
ENST00000334785.11:c.*51_*54delinsTTTC	ENSP00000333938.7:n.*51_*54delinsTTTC
ENST00000342754.5:c.1717-20_1717-17delinsTTTC
ENST00000480732.2:n.1653_1656delinsTTTC
NM_001172309.1:c.*51_*54delinsTTTC	NP_001165780.1:n.*51_*54delinsTTTC
NM_144573.3:c.*51_*54delinsTTTC , LRG_442t1:c.*51_*54delinsTTTC	NP_653174.3:n.*51_*54delinsTTTC
XM_005271322.2:c.2018-20_2018-17delinsTTTC	XP_005271379.1:n.2018-20_2018-17delinsTTTC
XM_005271323.2:c.1976-20_1976-17delinsTTTC	XP_005271380.1:n.1976-20_1976-17delinsTTTC
XM_005271324.3:c.1826-20_1826-17delinsTTTC	XP_005271381.1:n.1826-20_1826-17delinsTTTC
XM_005271325.2:c.1796-20_1796-17delinsTTTC	XP_005271382.1:n.1796-20_1796-17delinsTTTC
XM_005271326.2:c.1784-20_1784-17delinsTTTC	XP_005271383.1:n.1784-20_1784-17delinsTTTC
XM_005271327.2:c.1601-20_1601-17delinsTTTC	XP_005271384.1:n.1601-20_1601-17delinsTTTC
XM_005271322.4:c.2018-20_2018-17delinsTTTC	XP_005271379.1:n.2018-20_2018-17delinsTTTC
XM_005271323.4:c.1976-20_1976-17delinsTTTC	XP_005271380.1:n.1976-20_1976-17delinsTTTC
XM_005271324.5:c.1826-20_1826-17delinsTTTC	XP_005271381.1:n.1826-20_1826-17delinsTTTC
XM_005271325.4:c.1796-20_1796-17delinsTTTC	XP_005271382.1:n.1796-20_1796-17delinsTTTC
XM_005271326.4:c.1784-20_1784-17delinsTTTC	XP_005271383.1:n.1784-20_1784-17delinsTTTC
XM_005271327.4:c.1601-20_1601-17delinsTTTC	XP_005271384.1:n.1601-20_1601-17delinsTTTC
NM_001172309.2:c.*51_*54delinsTTTC	NP_001165780.1:n.*51_*54delinsTTTC
NM_144573.4:c.*51_*54delinsTTTC MANE Select	NP_653174.3:n.*51_*54delinsTTTC