Canonical Allele Identifier: CA425358028

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26414410T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191541T>A , CM000664.2:g.26191541T>A	GRCh38
NC_000002.11:g.26414410T>A , CM000664.1:g.26414410T>A	GRCh37
NC_000002.10:g.26267914T>A	NCBI36
NG_007121.1:g.58080A>T
NG_007121.2:g.58081A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2088A>T (HADHA) MANE Select	ENSP00000370023.3:p.Thr696=
ENST00000492433.2:c.2088A>T (HADHA)	ENSP00000438039.2:p.Thr696=
ENST00000643057.1:c.*1979A>T (HADHA)	ENSP00000493761.1:n.*1979A>T
ENST00000643063.1:c.*1134A>T (HADHA)	ENSP00000495353.1:n.*1134A>T
ENST00000643233.1:c.*1979A>T (HADHA)	ENSP00000493880.1:n.*1979A>T
ENST00000644428.1:c.*712A>T (HADHA)	ENSP00000495560.1:n.*712A>T
ENST00000645274.1:c.1983A>T (HADHA)	ENSP00000493996.1:p.Thr661=
ENST00000646031.1:c.1447A>T (HADHA)
ENST00000646483.1:c.1954A>T (HADHA)	ENSP00000496185.1:n.1954A>T
ENST00000380649.7:c.2088A>T (HADHA)	ENSP00000370023.3:p.Thr696=
ENST00000492433.1:c.546A>T (HADHA)	ENSP00000438039.1:p.Thr182=
NM_000182.4:c.2088A>T (HADHA)	NP_000173.2:p.Thr696=
XM_011532567.1:c.1683+4226T>A (GAREM2)	XP_011530869.1:n.1683+4226T>A
XM_011532567.3:c.1683+4226T>A (GAREM2)	XP_011530869.1:n.1683+4226T>A
NM_000182.5:c.2088A>T (HADHA) MANE Select	NP_000173.2:p.Thr696=