Canonical Allele Identifier: CA352517055
Gene: NBEAL2 HGNC NCBI

Linked Data

dbSNP Id: rs1437541636
gnomAD v2: 3-47041764-T-C
gnomAD v3: 3-47000274-T-C
gnomAD v4: 3-47000274-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47000274T>C , CM000665.2:g.47000274T>C GRCh38
NC_000003.11:g.47041764T>C , CM000665.1:g.47041764T>C GRCh37
NC_000003.10:g.47016768T>C NCBI36
NG_031914.1:g.25592T>C , LRG_568:g.25592T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450053.8:c.4175T>C MANE Select ENSP00000415034.2:p.Leu1392Pro
ENST00000651747.1:c.4073T>C ENSP00000499216.1:p.Leu1358Pro
ENST00000416683.5:c.2038T>C
ENST00000450053.7:c.4175T>C ENSP00000415034.2:p.Leu1392Pro
NM_015175.2:c.4175T>C , LRG_568t1:c.4175T>C NP_055990.1:p.Leu1392Pro
XM_005264992.2:c.4073T>C XP_005265049.1:p.Leu1358Pro
XM_005264993.2:c.647T>C XP_005265050.1:p.Leu216Pro
XM_006713072.2:c.4094T>C XP_006713135.1:p.Leu1365Pro
XM_011533532.1:c.4154T>C XP_011531834.1:p.Leu1385Pro
XM_011533533.1:c.4175T>C XP_011531835.1:p.Leu1392Pro
XM_011533534.1:c.3806T>C XP_011531836.1:p.Leu1269Pro
XM_011533535.1:c.3635T>C XP_011531837.1:p.Leu1212Pro
XM_011533536.1:c.3521T>C XP_011531838.1:p.Leu1174Pro
XM_011533537.1:c.3083T>C XP_011531839.1:p.Leu1028Pro
XR_940397.1:n.4351T>C
XR_940398.1:n.4351T>C
NM_001365116.1:c.4073T>C NP_001352045.1:p.Leu1358Pro
XM_006713072.3:c.4094T>C XP_006713135.1:p.Leu1365Pro
XM_011533533.2:c.4175T>C XP_011531835.1:p.Leu1392Pro
XM_017006010.1:c.4175T>C XP_016861499.1:p.Leu1392Pro
XM_017006011.1:c.4154T>C XP_016861500.1:p.Leu1385Pro
XM_017006012.1:c.4094T>C XP_016861501.1:p.Leu1365Pro
XM_017006013.1:c.4175T>C XP_016861502.1:p.Leu1392Pro
XM_017006014.1:c.4073T>C XP_016861503.1:p.Leu1358Pro
XM_017006015.1:c.3806T>C XP_016861504.1:p.Leu1269Pro
XM_017006016.1:c.3635T>C XP_016861505.1:p.Leu1212Pro
XM_017006017.1:c.647T>C XP_016861506.1:p.Leu216Pro
XR_940397.2:n.4351T>C
NM_001365116.2:c.4073T>C NP_001352045.1:p.Leu1358Pro
NM_015175.3:c.4175T>C MANE Select NP_055990.1:p.Leu1392Pro