Canonical Allele Identifier: CA425357996

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26414365C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191496C>G , CM000664.2:g.26191496C>G	GRCh38
NC_000002.11:g.26414365C>G , CM000664.1:g.26414365C>G	GRCh37
NC_000002.10:g.26267869C>G	NCBI36
NG_007121.1:g.58125G>C
NG_007121.2:g.58126G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.2133G>C (HADHA) MANE Select	ENSP00000370023.3:p.Pro711=
ENST00000492433.2:c.2133G>C (HADHA)	ENSP00000438039.2:p.Pro711=
ENST00000643057.1:c.*2024G>C (HADHA)	ENSP00000493761.1:n.*2024G>C
ENST00000643063.1:c.*1179G>C (HADHA)	ENSP00000495353.1:n.*1179G>C
ENST00000643233.1:c.*2024G>C (HADHA)	ENSP00000493880.1:n.*2024G>C
ENST00000644428.1:c.*757G>C (HADHA)	ENSP00000495560.1:n.*757G>C
ENST00000645274.1:c.2028G>C (HADHA)	ENSP00000493996.1:p.Pro676=
ENST00000646031.1:c.1492G>C (HADHA)
ENST00000646483.1:c.1999G>C (HADHA)	ENSP00000496185.1:n.1999G>C
ENST00000380649.7:c.2133G>C (HADHA)	ENSP00000370023.3:p.Pro711=
ENST00000492433.1:c.591G>C (HADHA)	ENSP00000438039.1:p.Pro197=
NM_000182.4:c.2133G>C (HADHA)	NP_000173.2:p.Pro711=
XM_011532567.1:c.1683+4181C>G (GAREM2)	XP_011530869.1:n.1683+4181C>G
XM_011532567.3:c.1683+4181C>G (GAREM2)	XP_011530869.1:n.1683+4181C>G
NM_000182.5:c.2133G>C (HADHA) MANE Select	NP_000173.2:p.Pro711=