Canonical Allele Identifier: CA1239700845

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191446G= , CM000664.2:g.26191446G=	GRCh38
NC_000002.11:g.26414315G= , CM000664.1:g.26414315G=	GRCh37
NC_000002.10:g.26267819G=	NCBI36
NG_007121.1:g.58175C=
NG_007121.2:g.58176C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2146+37C= (HADHA) MANE Select	ENSP00000370023.3:n.2146+37C=
ENST00000492433.2:c.2183C= (HADHA)	ENSP00000438039.2:p.Ala728=
ENST00000643057.1:c.*2074C= (HADHA)	ENSP00000493761.1:n.*2074C=
ENST00000643063.1:c.*1192+37C= (HADHA)	ENSP00000495353.1:n.*1192+37C=
ENST00000643233.1:c.*2037+37C= (HADHA)	ENSP00000493880.1:n.*2037+37C=
ENST00000644428.1:c.*770+37C= (HADHA)	ENSP00000495560.1:n.*770+37C=
ENST00000645274.1:c.2041+37C= (HADHA)	ENSP00000493996.1:n.2041+37C=
ENST00000646031.1:c.1505+37C= (HADHA)
ENST00000646483.1:c.2012+37C= (HADHA)	ENSP00000496185.1:n.2012+37C=
ENST00000380649.7:c.2146+37C= (HADHA)	ENSP00000370023.3:n.2146+37C=
ENST00000492433.1:c.641C= (HADHA)	ENSP00000438039.1:p.Ala214=
NM_000182.4:c.2146+37C= (HADHA)	NP_000173.2:n.2146+37C=
XM_011532567.1:c.1683+4131G= (GAREM2)	XP_011530869.1:n.1683+4131G=
XM_011532567.3:c.1683+4131G= (GAREM2)	XP_011530869.1:n.1683+4131G=
NM_000182.5:c.2146+37C= (HADHA) MANE Select	NP_000173.2:n.2146+37C=