Canonical Allele Identifier: CA346113095

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26414432A>G (hg19) ; chr2:g.26191563A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191563A>G , CM000664.2:g.26191563A>G	GRCh38
NC_000002.11:g.26414432A>G , CM000664.1:g.26414432A>G	GRCh37
NC_000002.10:g.26267936A>G	NCBI36
NG_007121.1:g.58058T>C
NG_007121.2:g.58059T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2066T>C (HADHA) MANE Select	ENSP00000370023.3:p.Leu689Pro
ENST00000492433.2:c.2066T>C (HADHA)	ENSP00000438039.2:p.Leu689Pro
ENST00000643057.1:c.*1957T>C (HADHA)	ENSP00000493761.1:n.*1957T>C
ENST00000643063.1:c.*1112T>C (HADHA)	ENSP00000495353.1:n.*1112T>C
ENST00000643233.1:c.*1957T>C (HADHA)	ENSP00000493880.1:n.*1957T>C
ENST00000644428.1:c.*690T>C (HADHA)	ENSP00000495560.1:n.*690T>C
ENST00000645274.1:c.1961T>C (HADHA)	ENSP00000493996.1:p.Leu654Pro
ENST00000646031.1:c.1425T>C (HADHA)
ENST00000646483.1:c.1932T>C (HADHA)	ENSP00000496185.1:n.1932T>C
ENST00000380649.7:c.2066T>C (HADHA)	ENSP00000370023.3:p.Leu689Pro
ENST00000492433.1:c.524T>C (HADHA)	ENSP00000438039.1:p.Leu175Pro
NM_000182.4:c.2066T>C (HADHA)	NP_000173.2:p.Leu689Pro
XM_011532567.1:c.1683+4248A>G (GAREM2)	XP_011530869.1:n.1683+4248A>G
XM_011532567.3:c.1683+4248A>G (GAREM2)	XP_011530869.1:n.1683+4248A>G
NM_000182.5:c.2066T>C (HADHA) MANE Select	NP_000173.2:p.Leu689Pro