Canonical Allele Identifier: CA2042817465

Gene: HMGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65965851_65965852delinsGA , CM000674.2:g.65965851_65965852delinsGA	GRCh38
NC_000012.11:g.66359631_66359632delinsGA , CM000674.1:g.66359631_66359632delinsGA	GRCh37
NC_000012.10:g.64645898_64645899delinsGA	NCBI36
NG_016296.1:g.146392_146393delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403681.7:c.*2559_*2560delinsGA MANE Select	ENSP00000384026.2:n.*2559_*2560delinsGA
ENST00000403681.6:c.*2559_*2560delinsGA	ENSP00000384026.2:n.*2559_*2560delinsGA
NM_003483.4:c.*2559_*2560delinsGA	NP_003474.1:n.*2559_*2560delinsGA
NM_003483.6:c.*2559_*2560delinsGA MANE Select	NP_003474.1:n.*2559_*2560delinsGA