Canonical Allele Identifier: CA2082579028

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872537_31872542delinsGGAAGT , CM000675.2:g.31872537_31872542delinsGGAAGT GRCh38
NC_000013.10:g.32446674_32446679delinsGGAAGT , CM000675.1:g.32446674_32446679delinsGGAAGT GRCh37
NC_000013.9:g.31344674_31344679delinsGGAAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645780.1:c.-254+25598_-254+25603delinsGGAAGT (FRY) ENSP00000494080.1:n.-254+25598_-254+25603delinsGGAAGT
ENST00000428783.1:n.99+25598_99+25603delinsGGAAGT (EEF1DP3)
NR_027062.1:n.157+25598_157+25603delinsGGAAGT (EEF1DP3)