Canonical Allele Identifier: CA425357861

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26414197A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191328A>C , CM000664.2:g.26191328A>C	GRCh38
NC_000002.11:g.26414197A>C , CM000664.1:g.26414197A>C	GRCh37
NC_000002.10:g.26267701A>C	NCBI36
NG_007121.1:g.58293T>G
NG_007121.2:g.58294T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2214T>G (HADHA) MANE Select	ENSP00000370023.3:p.Ala738=
ENST00000492433.2:c.2301T>G (HADHA)	ENSP00000438039.2:p.Ala767=
ENST00000643057.1:c.*2192T>G (HADHA)	ENSP00000493761.1:n.*2192T>G
ENST00000643063.1:c.*1260T>G (HADHA)	ENSP00000495353.1:n.*1260T>G
ENST00000643233.1:c.*2105T>G (HADHA)	ENSP00000493880.1:n.*2105T>G
ENST00000644428.1:c.*838T>G (HADHA)	ENSP00000495560.1:n.*838T>G
ENST00000645274.1:c.2109T>G (HADHA)	ENSP00000493996.1:p.Ala703=
ENST00000646031.1:c.1573T>G (HADHA)
ENST00000646483.1:c.2080T>G (HADHA)	ENSP00000496185.1:n.2080T>G
ENST00000380649.7:c.2214T>G (HADHA)	ENSP00000370023.3:p.Ala738=
NM_000182.4:c.2214T>G (HADHA)	NP_000173.2:p.Ala738=
XM_011532567.1:c.1683+4013A>C (GAREM2)	XP_011530869.1:n.1683+4013A>C
XM_011532567.3:c.1683+4013A>C (GAREM2)	XP_011530869.1:n.1683+4013A>C
NM_000182.5:c.2214T>G (HADHA) MANE Select	NP_000173.2:p.Ala738=