Canonical Allele Identifier: CA2082579061

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31872572_31872576delinsAATTT , CM000675.2:g.31872572_31872576delinsAATTT GRCh38
NC_000013.10:g.32446709_32446713delinsAATTT , CM000675.1:g.32446709_32446713delinsAATTT GRCh37
NC_000013.9:g.31344709_31344713delinsAATTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645780.1:c.-254+25633_-254+25637delinsAATTT (FRY) ENSP00000494080.1:n.-254+25633_-254+25637delinsAATTT
ENST00000428783.1:n.99+25633_99+25637delinsAATTT (EEF1DP3)
NR_027062.1:n.157+25633_157+25637delinsAATTT (EEF1DP3)