Canonical Allele Identifier: CA1559536

Gene: HADHA GAREM2

Linked Data

• ClinVar Variation Id: 2164512
• ClinVar RCV Id: RCV003082139 ; RCV003088069
• dbSNP Id: rs763333426
• ExAC: 2:26418043 G / A
• gnomAD v2: 2-26418043-G-A
• gnomAD v3: 2-26195174-G-A
• gnomAD v4: 2-26195174-G-A
• MyVariant Identifiers: chr2:g.26418043G>A (hg19) ; chr2:g.26195174G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26195174G>A , CM000664.2:g.26195174G>A	GRCh38
NC_000002.11:g.26418043G>A , CM000664.1:g.26418043G>A	GRCh37
NC_000002.10:g.26271547G>A	NCBI36
NG_007121.1:g.54447C>T
NG_007121.2:g.54448C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1538C>T (HADHA) MANE Select	ENSP00000370023.3:p.Thr513Met
ENST00000492433.2:c.1538C>T (HADHA)	ENSP00000438039.2:p.Thr513Met
ENST00000643057.1:c.*1429C>T (HADHA)	ENSP00000493761.1:n.*1429C>T
ENST00000643063.1:c.*584C>T (HADHA)	ENSP00000495353.1:n.*584C>T
ENST00000643233.1:c.*1429C>T (HADHA)	ENSP00000493880.1:n.*1429C>T
ENST00000644428.1:c.*162C>T (HADHA)	ENSP00000495560.1:n.*162C>T
ENST00000645274.1:c.1433C>T (HADHA)	ENSP00000493996.1:p.Thr478Met
ENST00000646031.1:c.897C>T (HADHA)
ENST00000646483.1:c.1404C>T (HADHA)	ENSP00000496185.1:n.1404C>T
ENST00000380649.7:c.1538C>T (HADHA)	ENSP00000370023.3:p.Thr513Met
NM_000182.4:c.1538C>T (HADHA)	NP_000173.2:p.Thr513Met
XM_011532567.1:c.1684-7059G>A (GAREM2)	XP_011530869.1:n.1684-7059G>A
XM_011532567.3:c.1684-7059G>A (GAREM2)	XP_011530869.1:n.1684-7059G>A
NM_000182.5:c.1538C>T (HADHA) MANE Select	NP_000173.2:p.Thr513Met