Canonical Allele Identifier: CA2244625839

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933901_4933934delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG , CM000679.2:g.4933901_4933934delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG GRCh38
NC_000017.10:g.4837196_4837229delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG , CM000679.1:g.4837196_4837229delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG GRCh37
NG_008767.2:g.6607_6640delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1297_1330delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG (GP1BA) MANE Select ENSP00000329380.5:p.Ser433=
ENST00000649830.1:c.-888+408_-888+441delinsCGGGCTCTGAGGTGGGCTCTGGGGTGGTCGGGCT (CHRNE) ENSP00000496907.1:n.-888+408_-888+441delinsCGGGCTCTGAGGTGGGCT...
ENST00000329125.5:c.1297_1330delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG (GP1BA) ENSP00000329380.5:p.Ser433=
ENST00000611961.1:c.1272+25_1273-21delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG (GP1BA) ENSP00000484439.1:n.1272+25_1273-21delinsAGCCCGACCACCCCAGAGCC...
NM_000173.6:c.1297_1330delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG (GP1BA) NP_000164.5:p.Ser433=
NM_000173.7:c.1297_1330delinsAGCCCGACCACCCCAGAGCCCACCTCAGAGCCCG (GP1BA) MANE Select NP_000164.5:p.Ser433=