Canonical Allele Identifier: CA1362363056
Gene: NBEAL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47000182_47000183delinsAC , CM000665.2:g.47000182_47000183delinsAC GRCh38
NC_000003.11:g.47041672_47041673delinsAC , CM000665.1:g.47041672_47041673delinsAC GRCh37
NC_000003.10:g.47016676_47016677delinsAC NCBI36
NG_031914.1:g.25500_25501delinsAC , LRG_568:g.25500_25501delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000450053.8:c.4083_4084delinsAC MANE Select ENSP00000415034.2:p.Glu1361=
ENST00000651747.1:c.3981_3982delinsAC ENSP00000499216.1:p.Glu1327=
ENST00000652744.1:n.420_421delinsAC
ENST00000416683.5:c.1960-14_1960-13delinsAC
ENST00000450053.7:c.4083_4084delinsAC ENSP00000415034.2:p.Glu1361=
NM_015175.2:c.4083_4084delinsAC , LRG_568t1:c.4083_4084delinsAC NP_055990.1:p.Glu1361=
XM_005264992.2:c.3981_3982delinsAC XP_005265049.1:p.Glu1327=
XM_005264993.2:c.555_556delinsAC XP_005265050.1:p.Glu185=
XM_006713072.2:c.4002_4003delinsAC XP_006713135.1:p.Glu1334=
XM_011533532.1:c.4062_4063delinsAC XP_011531834.1:p.Glu1354=
XM_011533533.1:c.4083_4084delinsAC XP_011531835.1:p.Glu1361=
XM_011533534.1:c.3714_3715delinsAC XP_011531836.1:p.Glu1238=
XM_011533535.1:c.3543_3544delinsAC XP_011531837.1:p.Glu1181=
XM_011533536.1:c.3429_3430delinsAC XP_011531838.1:p.Glu1143=
XM_011533537.1:c.2991_2992delinsAC XP_011531839.1:p.Glu997=
XR_940397.1:n.4259_4260delinsAC
XR_940398.1:n.4259_4260delinsAC
NM_001365116.1:c.3981_3982delinsAC NP_001352045.1:p.Glu1327=
XM_006713072.3:c.4002_4003delinsAC XP_006713135.1:p.Glu1334=
XM_011533533.2:c.4083_4084delinsAC XP_011531835.1:p.Glu1361=
XM_017006010.1:c.4083_4084delinsAC XP_016861499.1:p.Glu1361=
XM_017006011.1:c.4062_4063delinsAC XP_016861500.1:p.Glu1354=
XM_017006012.1:c.4002_4003delinsAC XP_016861501.1:p.Glu1334=
XM_017006013.1:c.4083_4084delinsAC XP_016861502.1:p.Glu1361=
XM_017006014.1:c.3981_3982delinsAC XP_016861503.1:p.Glu1327=
XM_017006015.1:c.3714_3715delinsAC XP_016861504.1:p.Glu1238=
XM_017006016.1:c.3543_3544delinsAC XP_016861505.1:p.Glu1181=
XM_017006017.1:c.555_556delinsAC XP_016861506.1:p.Glu185=
XR_940397.2:n.4259_4260delinsAC
NM_001365116.2:c.3981_3982delinsAC NP_001352045.1:p.Glu1327=
NM_015175.3:c.4083_4084delinsAC MANE Select NP_055990.1:p.Glu1361=