Canonical Allele Identifier: CA2042782656

Gene: HMGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65949728_65949729delinsAT , CM000674.2:g.65949728_65949729delinsAT	GRCh38
NC_000012.11:g.66343508_66343509delinsAT , CM000674.1:g.66343508_66343509delinsAT	GRCh37
NC_000012.10:g.64629775_64629776delinsAT	NCBI36
NG_016296.1:g.130269_130270delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403681.7:c.250-1655_250-1654delinsAT MANE Select	ENSP00000384026.2:n.250-1655_250-1654delinsAT
ENST00000393577.7:c.250-1655_250-1654delinsAT	ENSP00000377205.3:n.250-1655_250-1654delinsAT
ENST00000403681.6:c.250-1655_250-1654delinsAT	ENSP00000384026.2:n.250-1655_250-1654delinsAT
ENST00000539662.1:c.287-1655_287-1654delinsAT	ENSP00000440919.1:n.287-1655_287-1654delinsAT
ENST00000541363.5:c.250-1655_250-1654delinsAT	ENSP00000439317.1:n.250-1655_250-1654delinsAT
NM_001300918.1:c.250-1655_250-1654delinsAT	NP_001287847.1:n.250-1655_250-1654delinsAT
NM_003483.4:c.250-1655_250-1654delinsAT	NP_003474.1:n.250-1655_250-1654delinsAT
NM_003483.6:c.250-1655_250-1654delinsAT MANE Select	NP_003474.1:n.250-1655_250-1654delinsAT