Canonical Allele Identifier: CA1362363090
Gene: NBEAL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47000257C= , CM000665.2:g.47000257C= GRCh38
NC_000003.11:g.47041747C= , CM000665.1:g.47041747C= GRCh37
NC_000003.10:g.47016751C= NCBI36
NG_031914.1:g.25575C= , LRG_568:g.25575C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000450053.8:c.4158C= MANE Select ENSP00000415034.2:p.Pro1386=
ENST00000651747.1:c.4056C= ENSP00000499216.1:p.Pro1352=
ENST00000416683.5:c.2021C=
ENST00000450053.7:c.4158C= ENSP00000415034.2:p.Pro1386=
NM_015175.2:c.4158C= , LRG_568t1:c.4158C= NP_055990.1:p.Pro1386=
XM_005264992.2:c.4056C= XP_005265049.1:p.Pro1352=
XM_005264993.2:c.630C= XP_005265050.1:p.Pro210=
XM_006713072.2:c.4077C= XP_006713135.1:p.Pro1359=
XM_011533532.1:c.4137C= XP_011531834.1:p.Pro1379=
XM_011533533.1:c.4158C= XP_011531835.1:p.Pro1386=
XM_011533534.1:c.3789C= XP_011531836.1:p.Pro1263=
XM_011533535.1:c.3618C= XP_011531837.1:p.Pro1206=
XM_011533536.1:c.3504C= XP_011531838.1:p.Pro1168=
XM_011533537.1:c.3066C= XP_011531839.1:p.Pro1022=
XR_940397.1:n.4334C=
XR_940398.1:n.4334C=
NM_001365116.1:c.4056C= NP_001352045.1:p.Pro1352=
XM_006713072.3:c.4077C= XP_006713135.1:p.Pro1359=
XM_011533533.2:c.4158C= XP_011531835.1:p.Pro1386=
XM_017006010.1:c.4158C= XP_016861499.1:p.Pro1386=
XM_017006011.1:c.4137C= XP_016861500.1:p.Pro1379=
XM_017006012.1:c.4077C= XP_016861501.1:p.Pro1359=
XM_017006013.1:c.4158C= XP_016861502.1:p.Pro1386=
XM_017006014.1:c.4056C= XP_016861503.1:p.Pro1352=
XM_017006015.1:c.3789C= XP_016861504.1:p.Pro1263=
XM_017006016.1:c.3618C= XP_016861505.1:p.Pro1206=
XM_017006017.1:c.630C= XP_016861506.1:p.Pro210=
XR_940397.2:n.4334C=
NM_001365116.2:c.4056C= NP_001352045.1:p.Pro1352=
NM_015175.3:c.4158C= MANE Select NP_055990.1:p.Pro1386=