Canonical Allele Identifier: CA2518482810
Gene: HMGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964642_65964643insAAC , CM000674.2:g.65964642_65964643insAAC GRCh38
NC_000012.11:g.66358422_66358423insAAC , CM000674.1:g.66358422_66358423insAAC GRCh37
NC_000012.10:g.64644689_64644690insAAC NCBI36
NG_016296.1:g.145183_145184insAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1350_*1351insAAC MANE Select ENSP00000384026.2:n.*1350_*1351insAAC
ENST00000403681.6:c.*1350_*1351insAAC ENSP00000384026.2:n.*1350_*1351insAAC
NM_003483.4:c.*1350_*1351insAAC NP_003474.1:n.*1350_*1351insAAC
NM_003483.6:c.*1350_*1351insAAC MANE Select NP_003474.1:n.*1350_*1351insAAC