Canonical Allele Identifier: CA1239701251

Gene: HADHA GAREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192341C= , CM000664.2:g.26192341C=	GRCh38
NC_000002.11:g.26415210C= , CM000664.1:g.26415210C=	GRCh37
NC_000002.10:g.26268714C=	NCBI36
NG_007121.1:g.57280G=
NG_007121.2:g.57281G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1969G= (HADHA) MANE Select	ENSP00000370023.3:p.Ala657=
ENST00000492433.2:c.1969G= (HADHA)	ENSP00000438039.2:p.Ala657=
ENST00000643057.1:c.*1860G= (HADHA)	ENSP00000493761.1:n.*1860G=
ENST00000643063.1:c.*1015G= (HADHA)	ENSP00000495353.1:n.*1015G=
ENST00000643233.1:c.*1860G= (HADHA)	ENSP00000493880.1:n.*1860G=
ENST00000644428.1:c.*593G= (HADHA)	ENSP00000495560.1:n.*593G=
ENST00000645274.1:c.1864G= (HADHA)	ENSP00000493996.1:p.Ala622=
ENST00000646031.1:c.1328G= (HADHA)
ENST00000646483.1:c.1835G= (HADHA)	ENSP00000496185.1:n.1835G=
ENST00000380649.7:c.1969G= (HADHA)	ENSP00000370023.3:p.Ala657=
ENST00000492433.1:c.427G= (HADHA)	ENSP00000438039.1:p.Ala143=
NM_000182.4:c.1969G= (HADHA)	NP_000173.2:p.Ala657=
XM_011532567.1:c.1683+5026C= (GAREM2)	XP_011530869.1:n.1683+5026C=
XM_011532567.3:c.1683+5026C= (GAREM2)	XP_011530869.1:n.1683+5026C=
NM_000182.5:c.1969G= (HADHA) MANE Select	NP_000173.2:p.Ala657=