Canonical Allele Identifier: CA1559418

Gene: HADHA GAREM2

Linked Data

• ClinVar Variation Id: 335375
• ClinVar RCV Id: RCV002480192
• dbSNP Id: rs545660610
• ExAC: 2:26415267 T / C
• gnomAD v2: 2-26415267-T-C
• gnomAD v3: 2-26192398-T-C
• gnomAD v4: 2-26192398-T-C
• MyVariant Identifiers: chr2:g.26415267T>C (hg19) ; chr2:g.26192398T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192398T>C , CM000664.2:g.26192398T>C	GRCh38
NC_000002.11:g.26415267T>C , CM000664.1:g.26415267T>C	GRCh37
NC_000002.10:g.26268771T>C	NCBI36
NG_007121.1:g.57223A>G
NG_007121.2:g.57224A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.1912A>G (HADHA) MANE Select	ENSP00000370023.3:p.Ile638Val
ENST00000492433.2:c.1912A>G (HADHA)	ENSP00000438039.2:p.Ile638Val
ENST00000643057.1:c.*1803A>G (HADHA)	ENSP00000493761.1:n.*1803A>G
ENST00000643063.1:c.*958A>G (HADHA)	ENSP00000495353.1:n.*958A>G
ENST00000643233.1:c.*1803A>G (HADHA)	ENSP00000493880.1:n.*1803A>G
ENST00000644428.1:c.*536A>G (HADHA)	ENSP00000495560.1:n.*536A>G
ENST00000645274.1:c.1807A>G (HADHA)	ENSP00000493996.1:p.Ile603Val
ENST00000646031.1:c.1271A>G (HADHA)
ENST00000646483.1:c.1778A>G (HADHA)	ENSP00000496185.1:n.1778A>G
ENST00000380649.7:c.1912A>G (HADHA)	ENSP00000370023.3:p.Ile638Val
ENST00000492433.1:c.370A>G (HADHA)	ENSP00000438039.1:p.Ile124Val
NM_000182.4:c.1912A>G (HADHA)	NP_000173.2:p.Ile638Val
XM_011532567.1:c.1683+5083T>C (GAREM2)	XP_011530869.1:n.1683+5083T>C
XM_011532567.3:c.1683+5083T>C (GAREM2)	XP_011530869.1:n.1683+5083T>C
NM_000182.5:c.1912A>G (HADHA) MANE Select	NP_000173.2:p.Ile638Val