Canonical Allele Identifier: CA352516359
Gene: NBEAL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47000021G>A , CM000665.2:g.47000021G>A GRCh38
NC_000003.11:g.47041511G>A , CM000665.1:g.47041511G>A GRCh37
NC_000003.10:g.47016515G>A NCBI36
NG_031914.1:g.25339G>A , LRG_568:g.25339G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000450053.8:c.3922G>A MANE Select ENSP00000415034.2:p.Glu1308Lys
ENST00000651747.1:c.3820G>A ENSP00000499216.1:p.Glu1274Lys
ENST00000652744.1:n.259G>A
ENST00000416683.5:c.1960-175G>A
ENST00000450053.7:c.3922G>A ENSP00000415034.2:p.Glu1308Lys
NM_015175.2:c.3922G>A , LRG_568t1:c.3922G>A NP_055990.1:p.Glu1308Lys
XM_005264992.2:c.3820G>A XP_005265049.1:p.Glu1274Lys
XM_005264993.2:c.394G>A XP_005265050.1:p.Glu132Lys
XM_006713072.2:c.3841G>A XP_006713135.1:p.Glu1281Lys
XM_011533532.1:c.3901G>A XP_011531834.1:p.Glu1301Lys
XM_011533533.1:c.3922G>A XP_011531835.1:p.Glu1308Lys
XM_011533534.1:c.3553G>A XP_011531836.1:p.Glu1185Lys
XM_011533535.1:c.3382G>A XP_011531837.1:p.Glu1128Lys
XM_011533536.1:c.3268G>A XP_011531838.1:p.Glu1090Lys
XM_011533537.1:c.2830G>A XP_011531839.1:p.Glu944Lys
XR_940397.1:n.4098G>A
XR_940398.1:n.4098G>A
NM_001365116.1:c.3820G>A NP_001352045.1:p.Glu1274Lys
XM_006713072.3:c.3841G>A XP_006713135.1:p.Glu1281Lys
XM_011533533.2:c.3922G>A XP_011531835.1:p.Glu1308Lys
XM_017006010.1:c.3922G>A XP_016861499.1:p.Glu1308Lys
XM_017006011.1:c.3901G>A XP_016861500.1:p.Glu1301Lys
XM_017006012.1:c.3841G>A XP_016861501.1:p.Glu1281Lys
XM_017006013.1:c.3922G>A XP_016861502.1:p.Glu1308Lys
XM_017006014.1:c.3820G>A XP_016861503.1:p.Glu1274Lys
XM_017006015.1:c.3553G>A XP_016861504.1:p.Glu1185Lys
XM_017006016.1:c.3382G>A XP_016861505.1:p.Glu1128Lys
XM_017006017.1:c.394G>A XP_016861506.1:p.Glu132Lys
XR_940397.2:n.4098G>A
NM_001365116.2:c.3820G>A NP_001352045.1:p.Glu1274Lys
NM_015175.3:c.3922G>A MANE Select NP_055990.1:p.Glu1308Lys