Canonical Allele Identifier: CA1177631226

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942251_77942252delinsTA , CM000663.2:g.77942251_77942252delinsTA	GRCh38
NC_000001.10:g.78407936_78407937delinsTA , CM000663.1:g.78407936_78407937delinsTA	GRCh37
NC_000001.9:g.78180524_78180525delinsTA	NCBI36
NG_016625.1:g.58737_58738delinsTA , LRG_442:g.58737_58738delinsTA
NG_033243.2:g.41842_41843delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1659+43_1659+44delinsTA MANE Select	ENSP00000333938.7:n.1659+43_1659+44delinsTA
ENST00000330010.12:c.1467+43_1467+44delinsTA	ENSP00000327363.8:n.1467+43_1467+44delinsTA
ENST00000334785.11:c.1659+43_1659+44delinsTA	ENSP00000333938.7:n.1659+43_1659+44delinsTA
ENST00000342754.5:c.1358+43_1358+44delinsTA
ENST00000470735.1:n.498+43_498+44delinsTA
ENST00000480732.2:n.1233+43_1233+44delinsTA
NM_001172309.1:c.1467+43_1467+44delinsTA	NP_001165780.1:n.1467+43_1467+44delinsTA
NM_144573.3:c.1659+43_1659+44delinsTA , LRG_442t1:c.1659+43_1659+44delinsTA	NP_653174.3:n.1659+43_1659+44delinsTA
XM_005271322.2:c.1659+43_1659+44delinsTA	XP_005271379.1:n.1659+43_1659+44delinsTA
XM_005271323.2:c.1617+43_1617+44delinsTA	XP_005271380.1:n.1617+43_1617+44delinsTA
XM_005271324.3:c.1467+43_1467+44delinsTA	XP_005271381.1:n.1467+43_1467+44delinsTA
XM_005271325.2:c.1437+43_1437+44delinsTA	XP_005271382.1:n.1437+43_1437+44delinsTA
XM_005271326.2:c.1425+43_1425+44delinsTA	XP_005271383.1:n.1425+43_1425+44delinsTA
XM_005271327.2:c.1242+43_1242+44delinsTA	XP_005271384.1:n.1242+43_1242+44delinsTA
XM_005271322.4:c.1659+43_1659+44delinsTA	XP_005271379.1:n.1659+43_1659+44delinsTA
XM_005271323.4:c.1617+43_1617+44delinsTA	XP_005271380.1:n.1617+43_1617+44delinsTA
XM_005271324.5:c.1467+43_1467+44delinsTA	XP_005271381.1:n.1467+43_1467+44delinsTA
XM_005271325.4:c.1437+43_1437+44delinsTA	XP_005271382.1:n.1437+43_1437+44delinsTA
XM_005271326.4:c.1425+43_1425+44delinsTA	XP_005271383.1:n.1425+43_1425+44delinsTA
XM_005271327.4:c.1242+43_1242+44delinsTA	XP_005271384.1:n.1242+43_1242+44delinsTA
NM_001172309.2:c.1467+43_1467+44delinsTA	NP_001165780.1:n.1467+43_1467+44delinsTA
NM_144573.4:c.1659+43_1659+44delinsTA MANE Select	NP_653174.3:n.1659+43_1659+44delinsTA