Canonical Allele Identifier: CA1177631438

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942689_77942690delinsTA , CM000663.2:g.77942689_77942690delinsTA	GRCh38
NC_000001.10:g.78408374_78408375delinsTA , CM000663.1:g.78408374_78408375delinsTA	GRCh37
NC_000001.9:g.78180962_78180963delinsTA	NCBI36
NG_016625.1:g.59175_59176delinsTA , LRG_442:g.59175_59176delinsTA
NG_033243.2:g.41404_41405delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1888_1889delinsTA MANE Select	ENSP00000333938.7:p.Tyr630=
ENST00000330010.12:c.1696_1697delinsTA	ENSP00000327363.8:p.Tyr566=
ENST00000334785.11:c.1888_1889delinsTA	ENSP00000333938.7:p.Tyr630=
ENST00000342754.5:c.1587_1588delinsTA
ENST00000470735.1:n.727_728delinsTA
ENST00000480732.2:n.1462_1463delinsTA
NM_001172309.1:c.1696_1697delinsTA	NP_001165780.1:p.Tyr566=
NM_144573.3:c.1888_1889delinsTA , LRG_442t1:c.1888_1889delinsTA	NP_653174.3:p.Tyr630=
XM_005271322.2:c.1888_1889delinsTA	XP_005271379.1:p.Tyr630=
XM_005271323.2:c.1846_1847delinsTA	XP_005271380.1:p.Tyr616=
XM_005271324.3:c.1696_1697delinsTA	XP_005271381.1:p.Tyr566=
XM_005271325.2:c.1666_1667delinsTA	XP_005271382.1:p.Tyr556=
XM_005271326.2:c.1654_1655delinsTA	XP_005271383.1:p.Tyr552=
XM_005271327.2:c.1471_1472delinsTA	XP_005271384.1:p.Tyr491=
XM_005271322.4:c.1888_1889delinsTA	XP_005271379.1:p.Tyr630=
XM_005271323.4:c.1846_1847delinsTA	XP_005271380.1:p.Tyr616=
XM_005271324.5:c.1696_1697delinsTA	XP_005271381.1:p.Tyr566=
XM_005271325.4:c.1666_1667delinsTA	XP_005271382.1:p.Tyr556=
XM_005271326.4:c.1654_1655delinsTA	XP_005271383.1:p.Tyr552=
XM_005271327.4:c.1471_1472delinsTA	XP_005271384.1:p.Tyr491=
NM_001172309.2:c.1696_1697delinsTA	NP_001165780.1:p.Tyr566=
NM_144573.4:c.1888_1889delinsTA MANE Select	NP_653174.3:p.Tyr630=