Canonical Allele Identifier: CA1239700726

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191219G= , CM000664.2:g.26191219G=	GRCh38
NC_000002.11:g.26414088G= , CM000664.1:g.26414088G=	GRCh37
NC_000002.10:g.26267592G=	NCBI36
NG_007121.1:g.58402C=
NG_007121.2:g.58403C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.*31C= (HADHA) MANE Select	ENSP00000370023.3:n.*31C=
ENST00000492433.2:c.*31C= (HADHA)	ENSP00000438039.2:n.*31C=
ENST00000643057.1:c.*2301C= (HADHA)	ENSP00000493761.1:n.*2301C=
ENST00000643063.1:c.*1369C= (HADHA)	ENSP00000495353.1:n.*1369C=
ENST00000643233.1:c.*2214C= (HADHA)	ENSP00000493880.1:n.*2214C=
ENST00000644428.1:c.*947C= (HADHA)	ENSP00000495560.1:n.*947C=
ENST00000645274.1:c.*31C= (HADHA)	ENSP00000493996.1:n.*31C=
ENST00000646031.1:c.1682C= (HADHA)
ENST00000380649.7:c.*31C= (HADHA)	ENSP00000370023.3:n.*31C=
NM_000182.4:c.*31C= (HADHA)	NP_000173.2:n.*31C=
XM_011532567.1:c.1683+3904G= (GAREM2)	XP_011530869.1:n.1683+3904G=
XM_011532567.3:c.1683+3904G= (GAREM2)	XP_011530869.1:n.1683+3904G=
NM_000182.5:c.*31C= (HADHA) MANE Select	NP_000173.2:n.*31C=