Canonical Allele Identifier: CA425357826

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26414166G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191297G>A , CM000664.2:g.26191297G>A	GRCh38
NC_000002.11:g.26414166G>A , CM000664.1:g.26414166G>A	GRCh37
NC_000002.10:g.26267670G>A	NCBI36
NG_007121.1:g.58324C>T
NG_007121.2:g.58325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2245C>T (HADHA) MANE Select	ENSP00000370023.3:p.Leu749=
ENST00000492433.2:c.2332C>T (HADHA)	ENSP00000438039.2:p.Leu778=
ENST00000643057.1:c.*2223C>T (HADHA)	ENSP00000493761.1:n.*2223C>T
ENST00000643063.1:c.*1291C>T (HADHA)	ENSP00000495353.1:n.*1291C>T
ENST00000643233.1:c.*2136C>T (HADHA)	ENSP00000493880.1:n.*2136C>T
ENST00000644428.1:c.*869C>T (HADHA)	ENSP00000495560.1:n.*869C>T
ENST00000645274.1:c.2140C>T (HADHA)	ENSP00000493996.1:p.Leu714=
ENST00000646031.1:c.1604C>T (HADHA)
ENST00000646483.1:c.2111C>T (HADHA)	ENSP00000496185.1:n.2111C>T
ENST00000380649.7:c.2245C>T (HADHA)	ENSP00000370023.3:p.Leu749=
NM_000182.4:c.2245C>T (HADHA)	NP_000173.2:p.Leu749=
XM_011532567.1:c.1683+3982G>A (GAREM2)	XP_011530869.1:n.1683+3982G>A
XM_011532567.3:c.1683+3982G>A (GAREM2)	XP_011530869.1:n.1683+3982G>A
NM_000182.5:c.2245C>T (HADHA) MANE Select	NP_000173.2:p.Leu749=