Canonical Allele Identifier: CA1239700828

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191421G= , CM000664.2:g.26191421G=	GRCh38
NC_000002.11:g.26414290G= , CM000664.1:g.26414290G=	GRCh37
NC_000002.10:g.26267794G=	NCBI36
NG_007121.1:g.58200C=
NG_007121.2:g.58201C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2147-26C= (HADHA) MANE Select	ENSP00000370023.3:n.2147-26C=
ENST00000492433.2:c.2208C= (HADHA)	ENSP00000438039.2:p.Phe736=
ENST00000643057.1:c.*2099C= (HADHA)	ENSP00000493761.1:n.*2099C=
ENST00000643063.1:c.*1193-26C= (HADHA)	ENSP00000495353.1:n.*1193-26C=
ENST00000643233.1:c.*2038-26C= (HADHA)	ENSP00000493880.1:n.*2038-26C=
ENST00000644428.1:c.*771-26C= (HADHA)	ENSP00000495560.1:n.*771-26C=
ENST00000645274.1:c.2042-26C= (HADHA)	ENSP00000493996.1:n.2042-26C=
ENST00000646031.1:c.1506-26C= (HADHA)
ENST00000646483.1:c.2013-26C= (HADHA)	ENSP00000496185.1:n.2013-26C=
ENST00000380649.7:c.2147-26C= (HADHA)	ENSP00000370023.3:n.2147-26C=
ENST00000492433.1:c.666C= (HADHA)	ENSP00000438039.1:p.Phe222=
NM_000182.4:c.2147-26C= (HADHA)	NP_000173.2:n.2147-26C=
XM_011532567.1:c.1683+4106G= (GAREM2)	XP_011530869.1:n.1683+4106G=
XM_011532567.3:c.1683+4106G= (GAREM2)	XP_011530869.1:n.1683+4106G=
NM_000182.5:c.2147-26C= (HADHA) MANE Select	NP_000173.2:n.2147-26C=