Canonical Allele Identifier: CA2042782563

Gene: HMGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65949654_65949655delinsCA , CM000674.2:g.65949654_65949655delinsCA	GRCh38
NC_000012.11:g.66343434_66343435delinsCA , CM000674.1:g.66343434_66343435delinsCA	GRCh37
NC_000012.10:g.64629701_64629702delinsCA	NCBI36
NG_016296.1:g.130195_130196delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403681.7:c.250-1729_250-1728delinsCA MANE Select	ENSP00000384026.2:n.250-1729_250-1728delinsCA
ENST00000393577.7:c.250-1729_250-1728delinsCA	ENSP00000377205.3:n.250-1729_250-1728delinsCA
ENST00000403681.6:c.250-1729_250-1728delinsCA	ENSP00000384026.2:n.250-1729_250-1728delinsCA
ENST00000539662.1:c.287-1729_287-1728delinsCA	ENSP00000440919.1:n.287-1729_287-1728delinsCA
ENST00000541363.5:c.250-1729_250-1728delinsCA	ENSP00000439317.1:n.250-1729_250-1728delinsCA
NM_001300918.1:c.250-1729_250-1728delinsCA	NP_001287847.1:n.250-1729_250-1728delinsCA
NM_003483.4:c.250-1729_250-1728delinsCA	NP_003474.1:n.250-1729_250-1728delinsCA
NM_003483.6:c.250-1729_250-1728delinsCA MANE Select	NP_003474.1:n.250-1729_250-1728delinsCA