Canonical Allele Identifier: CA1239701242

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192320T= , CM000664.2:g.26192320T=	GRCh38
NC_000002.11:g.26415189T= , CM000664.1:g.26415189T=	GRCh37
NC_000002.10:g.26268693T=	NCBI36
NG_007121.1:g.57301A=
NG_007121.2:g.57302A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1990A= (HADHA) MANE Select	ENSP00000370023.3:p.Lys664=
ENST00000492433.2:c.1990A= (HADHA)	ENSP00000438039.2:p.Lys664=
ENST00000643057.1:c.*1881A= (HADHA)	ENSP00000493761.1:n.*1881A=
ENST00000643063.1:c.*1036A= (HADHA)	ENSP00000495353.1:n.*1036A=
ENST00000643233.1:c.*1881A= (HADHA)	ENSP00000493880.1:n.*1881A=
ENST00000644428.1:c.*614A= (HADHA)	ENSP00000495560.1:n.*614A=
ENST00000645274.1:c.1885A= (HADHA)	ENSP00000493996.1:p.Lys629=
ENST00000646031.1:c.1349A= (HADHA)
ENST00000646483.1:c.1856A= (HADHA)	ENSP00000496185.1:n.1856A=
ENST00000380649.7:c.1990A= (HADHA)	ENSP00000370023.3:p.Lys664=
ENST00000492433.1:c.448A= (HADHA)	ENSP00000438039.1:p.Lys150=
NM_000182.4:c.1990A= (HADHA)	NP_000173.2:p.Lys664=
XM_011532567.1:c.1683+5005T= (GAREM2)	XP_011530869.1:n.1683+5005T=
XM_011532567.3:c.1683+5005T= (GAREM2)	XP_011530869.1:n.1683+5005T=
NM_000182.5:c.1990A= (HADHA) MANE Select	NP_000173.2:p.Lys664=