Canonical Allele Identifier: CA2244625104

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932363_4932367delinsCCTGT , CM000679.2:g.4932363_4932367delinsCCTGT GRCh38
NC_000017.10:g.4835658_4835662delinsCCTGT , CM000679.1:g.4835658_4835662delinsCCTGT GRCh37
NC_000017.9:g.4776438_4776442delinsCCTGT NCBI36
NG_008767.2:g.5069_5073delinsCCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.-9_-7+2delinsCCTGT (GP1BA)
ENST00000649830.1:c.-888+1975_-888+1979delinsACAGG (CHRNE) ENSP00000496907.1:n.-888+1975_-888+1979delinsACAGG
ENST00000329125.5:c.-9_-7+2delinsCCTGT (GP1BA)
ENST00000611961.1:c.-9_-7+2delinsCCTGT (GP1BA)
NM_000173.6:c.-9_-7+2delinsCCTGT (GP1BA)
NM_000173.7:c.-9_-7+2delinsCCTGT (GP1BA)