Canonical Allele Identifier: CA2000590762
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166844_112166846delinsCAA , CM000673.2:g.112166844_112166846delinsCAA GRCh38
NC_000011.9:g.112037567_112037569delinsCAA , CM000673.1:g.112037567_112037569delinsCAA GRCh37
NC_000011.8:g.111542777_111542779delinsCAA NCBI36
NG_028143.1:g.2272_2274delinsTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3575_320-3573delinsCAA
ENST00000531744.5:c.315-3575_315-3573delinsCAA ENSP00000456957.1:n.315-3575_315-3573deli...
ENST00000532699.1:c.315-3575_315-3573delinsCAA ENSP00000456434.1:n.315-3575_315-3573deli...