Canonical Allele Identifier: CA1239700731

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191225T= , CM000664.2:g.26191225T=	GRCh38
NC_000002.11:g.26414094T= , CM000664.1:g.26414094T=	GRCh37
NC_000002.10:g.26267598T=	NCBI36
NG_007121.1:g.58396A=
NG_007121.2:g.58397A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.*25A= (HADHA) MANE Select	ENSP00000370023.3:n.*25A=
ENST00000492433.2:c.*25A= (HADHA)	ENSP00000438039.2:n.*25A=
ENST00000643057.1:c.*2295A= (HADHA)	ENSP00000493761.1:n.*2295A=
ENST00000643063.1:c.*1363A= (HADHA)	ENSP00000495353.1:n.*1363A=
ENST00000643233.1:c.*2208A= (HADHA)	ENSP00000493880.1:n.*2208A=
ENST00000644428.1:c.*941A= (HADHA)	ENSP00000495560.1:n.*941A=
ENST00000645274.1:c.*25A= (HADHA)	ENSP00000493996.1:n.*25A=
ENST00000646031.1:c.1676A= (HADHA)
ENST00000380649.7:c.*25A= (HADHA)	ENSP00000370023.3:n.*25A=
NM_000182.4:c.*25A= (HADHA)	NP_000173.2:n.*25A=
XM_011532567.1:c.1683+3910T= (GAREM2)	XP_011530869.1:n.1683+3910T=
XM_011532567.3:c.1683+3910T= (GAREM2)	XP_011530869.1:n.1683+3910T=
NM_000182.5:c.*25A= (HADHA) MANE Select	NP_000173.2:n.*25A=