Canonical Allele Identifier: CA1177631221

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942237_77942238delinsCA , CM000663.2:g.77942237_77942238delinsCA	GRCh38
NC_000001.10:g.78407922_78407923delinsCA , CM000663.1:g.78407922_78407923delinsCA	GRCh37
NC_000001.9:g.78180510_78180511delinsCA	NCBI36
NG_016625.1:g.58723_58724delinsCA , LRG_442:g.58723_58724delinsCA
NG_033243.2:g.41856_41857delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1659+29_1659+30delinsCA MANE Select	ENSP00000333938.7:n.1659+29_1659+30delinsCA
ENST00000330010.12:c.1467+29_1467+30delinsCA	ENSP00000327363.8:n.1467+29_1467+30delinsCA
ENST00000334785.11:c.1659+29_1659+30delinsCA	ENSP00000333938.7:n.1659+29_1659+30delinsCA
ENST00000342754.5:c.1358+29_1358+30delinsCA
ENST00000470735.1:n.498+29_498+30delinsCA
ENST00000480732.2:n.1233+29_1233+30delinsCA
NM_001172309.1:c.1467+29_1467+30delinsCA	NP_001165780.1:n.1467+29_1467+30delinsCA
NM_144573.3:c.1659+29_1659+30delinsCA , LRG_442t1:c.1659+29_1659+30delinsCA	NP_653174.3:n.1659+29_1659+30delinsCA
XM_005271322.2:c.1659+29_1659+30delinsCA	XP_005271379.1:n.1659+29_1659+30delinsCA
XM_005271323.2:c.1617+29_1617+30delinsCA	XP_005271380.1:n.1617+29_1617+30delinsCA
XM_005271324.3:c.1467+29_1467+30delinsCA	XP_005271381.1:n.1467+29_1467+30delinsCA
XM_005271325.2:c.1437+29_1437+30delinsCA	XP_005271382.1:n.1437+29_1437+30delinsCA
XM_005271326.2:c.1425+29_1425+30delinsCA	XP_005271383.1:n.1425+29_1425+30delinsCA
XM_005271327.2:c.1242+29_1242+30delinsCA	XP_005271384.1:n.1242+29_1242+30delinsCA
XM_005271322.4:c.1659+29_1659+30delinsCA	XP_005271379.1:n.1659+29_1659+30delinsCA
XM_005271323.4:c.1617+29_1617+30delinsCA	XP_005271380.1:n.1617+29_1617+30delinsCA
XM_005271324.5:c.1467+29_1467+30delinsCA	XP_005271381.1:n.1467+29_1467+30delinsCA
XM_005271325.4:c.1437+29_1437+30delinsCA	XP_005271382.1:n.1437+29_1437+30delinsCA
XM_005271326.4:c.1425+29_1425+30delinsCA	XP_005271383.1:n.1425+29_1425+30delinsCA
XM_005271327.4:c.1242+29_1242+30delinsCA	XP_005271384.1:n.1242+29_1242+30delinsCA
NM_001172309.2:c.1467+29_1467+30delinsCA	NP_001165780.1:n.1467+29_1467+30delinsCA
NM_144573.4:c.1659+29_1659+30delinsCA MANE Select	NP_653174.3:n.1659+29_1659+30delinsCA