Canonical Allele Identifier: CA1239700856

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191465C= , CM000664.2:g.26191465C=	GRCh38
NC_000002.11:g.26414334C= , CM000664.1:g.26414334C=	GRCh37
NC_000002.10:g.26267838C=	NCBI36
NG_007121.1:g.58156G=
NG_007121.2:g.58157G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2146+18G= (HADHA) MANE Select	ENSP00000370023.3:n.2146+18G=
ENST00000492433.2:c.2164G= (HADHA)	ENSP00000438039.2:p.Gly722=
ENST00000643057.1:c.*2055G= (HADHA)	ENSP00000493761.1:n.*2055G=
ENST00000643063.1:c.*1192+18G= (HADHA)	ENSP00000495353.1:n.*1192+18G=
ENST00000643233.1:c.*2037+18G= (HADHA)	ENSP00000493880.1:n.*2037+18G=
ENST00000644428.1:c.*770+18G= (HADHA)	ENSP00000495560.1:n.*770+18G=
ENST00000645274.1:c.2041+18G= (HADHA)	ENSP00000493996.1:n.2041+18G=
ENST00000646031.1:c.1505+18G= (HADHA)
ENST00000646483.1:c.2012+18G= (HADHA)	ENSP00000496185.1:n.2012+18G=
ENST00000380649.7:c.2146+18G= (HADHA)	ENSP00000370023.3:n.2146+18G=
ENST00000492433.1:c.622G= (HADHA)	ENSP00000438039.1:p.Gly208=
NM_000182.4:c.2146+18G= (HADHA)	NP_000173.2:n.2146+18G=
XM_011532567.1:c.1683+4150C= (GAREM2)	XP_011530869.1:n.1683+4150C=
XM_011532567.3:c.1683+4150C= (GAREM2)	XP_011530869.1:n.1683+4150C=
NM_000182.5:c.2146+18G= (HADHA) MANE Select	NP_000173.2:n.2146+18G=