Canonical Allele Identifier: CA2244625843

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933903_4933940delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA , CM000679.2:g.4933903_4933940delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA GRCh38
NC_000017.10:g.4837198_4837235delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA , CM000679.1:g.4837198_4837235delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA GRCh37
NG_008767.2:g.6609_6646delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1299_1336delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA (GP1BA) MANE Select ENSP00000329380.5:p.Ser433=
ENST00000649830.1:c.-888+402_-888+439delinsTGGGGGCGGGCTCTGAGGTGGGCTCTGGGGTGGTCGGG (CHRNE) ENSP00000496907.1:n.-888+402_-888+439delinsTGGGGGCGGGCTCTGAGG...
ENST00000329125.5:c.1299_1336delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA (GP1BA) ENSP00000329380.5:p.Ser433=
ENST00000611961.1:c.1272+27_1273-15delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA (GP1BA) ENSP00000484439.1:n.1272+27_1273-15delinsCCCGACCACCCCAGAGCCCA...
NM_000173.6:c.1299_1336delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA (GP1BA) NP_000164.5:p.Ser433=
NM_000173.7:c.1299_1336delinsCCCGACCACCCCAGAGCCCACCTCAGAGCCCGCCCCCA (GP1BA) MANE Select NP_000164.5:p.Ser433=