Canonical Allele Identifier: CA1239700734

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191229T= , CM000664.2:g.26191229T=	GRCh38
NC_000002.11:g.26414098T= , CM000664.1:g.26414098T=	GRCh37
NC_000002.10:g.26267602T=	NCBI36
NG_007121.1:g.58392A=
NG_007121.2:g.58393A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.*21A= (HADHA) MANE Select	ENSP00000370023.3:n.*21A=
ENST00000492433.2:c.*21A= (HADHA)	ENSP00000438039.2:n.*21A=
ENST00000643057.1:c.*2291A= (HADHA)	ENSP00000493761.1:n.*2291A=
ENST00000643063.1:c.*1359A= (HADHA)	ENSP00000495353.1:n.*1359A=
ENST00000643233.1:c.*2204A= (HADHA)	ENSP00000493880.1:n.*2204A=
ENST00000644428.1:c.*937A= (HADHA)	ENSP00000495560.1:n.*937A=
ENST00000645274.1:c.*21A= (HADHA)	ENSP00000493996.1:n.*21A=
ENST00000646031.1:c.1672A= (HADHA)
ENST00000380649.7:c.*21A= (HADHA)	ENSP00000370023.3:n.*21A=
NM_000182.4:c.*21A= (HADHA)	NP_000173.2:n.*21A=
XM_011532567.1:c.1683+3914T= (GAREM2)	XP_011530869.1:n.1683+3914T=
XM_011532567.3:c.1683+3914T= (GAREM2)	XP_011530869.1:n.1683+3914T=
NM_000182.5:c.*21A= (HADHA) MANE Select	NP_000173.2:n.*21A=