Canonical Allele Identifier: CA1239700867

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191482C= , CM000664.2:g.26191482C=	GRCh38
NC_000002.11:g.26414351C= , CM000664.1:g.26414351C=	GRCh37
NC_000002.10:g.26267855C=	NCBI36
NG_007121.1:g.58139G=
NG_007121.2:g.58140G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.2146+1G= (HADHA) MANE Select	ENSP00000370023.3:n.2146+1G=
ENST00000492433.2:c.2147G= (HADHA)	ENSP00000438039.2:p.Gly716=
ENST00000643057.1:c.*2038G= (HADHA)	ENSP00000493761.1:n.*2038G=
ENST00000643063.1:c.*1192+1G= (HADHA)	ENSP00000495353.1:n.*1192+1G=
ENST00000643233.1:c.*2037+1G= (HADHA)	ENSP00000493880.1:n.*2037+1G=
ENST00000644428.1:c.*770+1G= (HADHA)	ENSP00000495560.1:n.*770+1G=
ENST00000645274.1:c.2041+1G= (HADHA)	ENSP00000493996.1:n.2041+1G=
ENST00000646031.1:c.1505+1G= (HADHA)
ENST00000646483.1:c.2012+1G= (HADHA)	ENSP00000496185.1:n.2012+1G=
ENST00000380649.7:c.2146+1G= (HADHA)	ENSP00000370023.3:n.2146+1G=
ENST00000492433.1:c.605G= (HADHA)	ENSP00000438039.1:p.Gly202=
NM_000182.4:c.2146+1G= (HADHA)	NP_000173.2:n.2146+1G=
XM_011532567.1:c.1683+4167C= (GAREM2)	XP_011530869.1:n.1683+4167C=
XM_011532567.3:c.1683+4167C= (GAREM2)	XP_011530869.1:n.1683+4167C=
NM_000182.5:c.2146+1G= (HADHA) MANE Select	NP_000173.2:n.2146+1G=