Canonical Allele Identifier: CA655098210
Gene: HMGA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964625_65964626insT , CM000674.2:g.65964625_65964626insT GRCh38
NC_000012.11:g.66358405_66358406insT , CM000674.1:g.66358405_66358406insT GRCh37
NC_000012.10:g.64644672_64644673insT NCBI36
NG_016296.1:g.145166_145167insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1333_*1334insT MANE Select ENSP00000384026.2:n.*1333_*1334insT
ENST00000403681.6:c.*1333_*1334insT ENSP00000384026.2:n.*1333_*1334insT
NM_003483.4:c.*1333_*1334insT NP_003474.1:n.*1333_*1334insT
NM_003483.6:c.*1333_*1334insT MANE Select NP_003474.1:n.*1333_*1334insT