Canonical Allele Identifier: CA2479556639
Gene: SELENBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151372113_151372114delinsTG , CM000663.2:g.151372113_151372114delinsTG GRCh38
NC_000001.10:g.151344589_151344590delinsTG , CM000663.1:g.151344589_151344590delinsTG GRCh37
NC_000001.9:g.149611213_149611214delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368868.10:c.4+524_4+525delinsCA MANE Select ENSP00000357861.5:n.4+524_4+525delinsCA
ENST00000368868.9:c.4+524_4+525delinsCA ENSP00000357861.5:n.4+524_4+525delinsCA
ENST00000423070.5:c.-80+524_-80+525delinsCA ENSP00000416206.1:n.-80+524_-80+525delinsCA
ENST00000426705.6:c.-80+524_-80+525delinsCA ENSP00000397261.2:n.-80+524_-80+525delinsCA
ENST00000427977.6:c.4+524_4+525delinsCA ENSP00000412816.1:n.4+524_4+525delinsCA
ENST00000443708.5:c.4+524_4+525delinsCA ENSP00000402531.1:n.4+524_4+525delinsCA
ENST00000447402.7:c.4+524_4+525delinsCA ENSP00000413960.3:n.4+524_4+525delinsCA
ENST00000455397.5:c.4+524_4+525delinsCA ENSP00000395637.1:n.4+524_4+525delinsCA
ENST00000455839.5:c.4+524_4+525delinsCA ENSP00000390433.1:n.4+524_4+525delinsCA
ENST00000458566.5:c.4+524_4+525delinsCA ENSP00000406222.1:n.4+524_4+525delinsCA
ENST00000463664.5:n.57+524_57+525delinsCA
ENST00000470345.5:n.69+524_69+525delinsCA
ENST00000473693.5:n.68+524_68+525delinsCA
ENST00000474352.5:n.68+524_68+525delinsCA
ENST00000492643.5:n.70+524_70+525delinsCA
ENST00000493560.5:n.57+524_57+525delinsCA
ENST00000498494.1:n.54+524_54+525delinsCA
NM_001258288.1:c.4+524_4+525delinsCA NP_001245217.1:n.4+524_4+525delinsCA
NM_001258289.1:c.-80+524_-80+525delinsCA NP_001245218.1:n.-80+524_-80+525delinsCA
NM_003944.3:c.4+524_4+525delinsCA NP_003935.2:n.4+524_4+525delinsCA
XM_011510110.1:c.-35+524_-35+525delinsCA XP_011508412.1:n.-35+524_-35+525delinsCA
XR_921993.1:n.84+524_84+525delinsCA
XM_024450671.1:c.-1161+524_-1161+525delinsCA XP_024306439.1:n.-1161+524_-1161+525delinsCA
XR_002957987.1:n.88+524_88+525delinsCA
XR_921993.2:n.76+524_76+525delinsCA
NM_003944.4:c.4+524_4+525delinsCA MANE Select NP_003935.2:n.4+524_4+525delinsCA
NM_001258288.2:c.4+524_4+525delinsCA NP_001245217.1:n.4+524_4+525delinsCA
NM_001258289.2:c.-80+524_-80+525delinsCA NP_001245218.1:n.-80+524_-80+525delinsCA