Canonical Allele Identifier: CA1239701279

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192386C= , CM000664.2:g.26192386C=	GRCh38
NC_000002.11:g.26415255C= , CM000664.1:g.26415255C=	GRCh37
NC_000002.10:g.26268759C=	NCBI36
NG_007121.1:g.57235G=
NG_007121.2:g.57236G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1924G= (HADHA) MANE Select	ENSP00000370023.3:p.Gly642=
ENST00000492433.2:c.1924G= (HADHA)	ENSP00000438039.2:p.Gly642=
ENST00000643057.1:c.*1815G= (HADHA)	ENSP00000493761.1:n.*1815G=
ENST00000643063.1:c.*970G= (HADHA)	ENSP00000495353.1:n.*970G=
ENST00000643233.1:c.*1815G= (HADHA)	ENSP00000493880.1:n.*1815G=
ENST00000644428.1:c.*548G= (HADHA)	ENSP00000495560.1:n.*548G=
ENST00000645274.1:c.1819G= (HADHA)	ENSP00000493996.1:p.Gly607=
ENST00000646031.1:c.1283G= (HADHA)
ENST00000646483.1:c.1790G= (HADHA)	ENSP00000496185.1:n.1790G=
ENST00000380649.7:c.1924G= (HADHA)	ENSP00000370023.3:p.Gly642=
ENST00000492433.1:c.382G= (HADHA)	ENSP00000438039.1:p.Gly128=
NM_000182.4:c.1924G= (HADHA)	NP_000173.2:p.Gly642=
XM_011532567.1:c.1683+5071C= (GAREM2)	XP_011530869.1:n.1683+5071C=
XM_011532567.3:c.1683+5071C= (GAREM2)	XP_011530869.1:n.1683+5071C=
NM_000182.5:c.1924G= (HADHA) MANE Select	NP_000173.2:p.Gly642=