Canonical Allele Identifier: CA2244625848

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933907_4933945delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG , CM000679.2:g.4933907_4933945delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG GRCh38
NC_000017.10:g.4837202_4837240delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG , CM000679.1:g.4837202_4837240delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG GRCh37
NG_008767.2:g.6613_6651delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1303_1341delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG (GP1BA) MANE Select ENSP00000329380.5:p.Thr435=
ENST00000649830.1:c.-888+397_-888+435delinsCGGGCTGGGGGCGGGCTCTGAGGTGGGCTCTGGGGTGGT (CHRNE) ENSP00000496907.1:n.-888+397_-888+435delinsCGGGCTGGGGGCGGGCTC...
ENST00000329125.5:c.1303_1341delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG (GP1BA) ENSP00000329380.5:p.Thr435=
ENST00000611961.1:c.1272+31_1273-10delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG (GP1BA) ENSP00000484439.1:n.1272+31_1273-10delinsACCACCCCAGAGCCCACCTC...
NM_000173.6:c.1303_1341delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG (GP1BA) NP_000164.5:p.Thr435=
NM_000173.7:c.1303_1341delinsACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCAGCCCG (GP1BA) MANE Select NP_000164.5:p.Thr435=