Canonical Allele Identifier: CA2573550849
Gene: SELENBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151372232_151372233insCACCCACCCCTC , CM000663.2:g.151372232_151372233insCACCCACCCCTC GRCh38
NC_000001.10:g.151344708_151344709insCACCCACCCCTC , CM000663.1:g.151344708_151344709insCACCCACCCCTC GRCh37
NC_000001.9:g.149611332_149611333insCACCCACCCCTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368868.10:c.4+406_4+407insAGGGGTGGGTGG MANE Select ENSP00000357861.5:n.4+406_4+407insAGGGGTGGGTGG
ENST00000368868.9:c.4+406_4+407insAGGGGTGGGTGG ENSP00000357861.5:n.4+406_4+407insAGGGGTGGGTGG
ENST00000423070.5:c.-80+406_-80+407insAGGGGTGGGTGG ENSP00000416206.1:n.-80+406_-80+407insAGGGGTGGGTGG
ENST00000426705.6:c.-80+406_-80+407insAGGGGTGGGTGG ENSP00000397261.2:n.-80+406_-80+407insAGGGGTGGGTGG
ENST00000427977.6:c.4+406_4+407insAGGGGTGGGTGG ENSP00000412816.1:n.4+406_4+407insAGGGGTGGGTGG
ENST00000443708.5:c.4+406_4+407insAGGGGTGGGTGG ENSP00000402531.1:n.4+406_4+407insAGGGGTGGGTGG
ENST00000447402.7:c.4+406_4+407insAGGGGTGGGTGG ENSP00000413960.3:n.4+406_4+407insAGGGGTGGGTGG
ENST00000455397.5:c.4+406_4+407insAGGGGTGGGTGG ENSP00000395637.1:n.4+406_4+407insAGGGGTGGGTGG
ENST00000455839.5:c.4+406_4+407insAGGGGTGGGTGG ENSP00000390433.1:n.4+406_4+407insAGGGGTGGGTGG
ENST00000458566.5:c.4+406_4+407insAGGGGTGGGTGG ENSP00000406222.1:n.4+406_4+407insAGGGGTGGGTGG
ENST00000463664.5:n.57+406_57+407insAGGGGTGGGTGG
ENST00000470345.5:n.69+406_69+407insAGGGGTGGGTGG
ENST00000473693.5:n.68+406_68+407insAGGGGTGGGTGG
ENST00000474352.5:n.68+406_68+407insAGGGGTGGGTGG
ENST00000492643.5:n.70+406_70+407insAGGGGTGGGTGG
ENST00000493560.5:n.57+406_57+407insAGGGGTGGGTGG
ENST00000498494.1:n.54+406_54+407insAGGGGTGGGTGG
NM_001258288.1:c.4+406_4+407insAGGGGTGGGTGG NP_001245217.1:n.4+406_4+407insAGGGGTGGGTGG
NM_001258289.1:c.-80+406_-80+407insAGGGGTGGGTGG NP_001245218.1:n.-80+406_-80+407insAGGGGTGGGTGG
NM_003944.3:c.4+406_4+407insAGGGGTGGGTGG NP_003935.2:n.4+406_4+407insAGGGGTGGGTGG
XM_011510110.1:c.-35+406_-35+407insAGGGGTGGGTGG XP_011508412.1:n.-35+406_-35+407insAGGGGTGGGTGG
XR_921993.1:n.84+406_84+407insAGGGGTGGGTGG
XM_024450671.1:c.-1161+406_-1161+407insAGGGGTGGGTGG XP_024306439.1:n.-1161+406_-1161+407insAGGGGTGGGTGG
XR_002957987.1:n.88+406_88+407insAGGGGTGGGTGG
XR_921993.2:n.76+406_76+407insAGGGGTGGGTGG
NM_003944.4:c.4+406_4+407insAGGGGTGGGTGG MANE Select NP_003935.2:n.4+406_4+407insAGGGGTGGGTGG
NM_001258288.2:c.4+406_4+407insAGGGGTGGGTGG NP_001245217.1:n.4+406_4+407insAGGGGTGGGTGG
NM_001258289.2:c.-80+406_-80+407insAGGGGTGGGTGG NP_001245218.1:n.-80+406_-80+407insAGGGGTGGGTGG