Canonical Allele Identifier: CA346114625

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26415214A>C (hg19) ; chr2:g.26192345A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192345A>C , CM000664.2:g.26192345A>C	GRCh38
NC_000002.11:g.26415214A>C , CM000664.1:g.26415214A>C	GRCh37
NC_000002.10:g.26268718A>C	NCBI36
NG_007121.1:g.57276T>G
NG_007121.2:g.57277T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1965T>G (HADHA) MANE Select	ENSP00000370023.3:p.Ile655Met
ENST00000492433.2:c.1965T>G (HADHA)	ENSP00000438039.2:p.Ile655Met
ENST00000643057.1:c.*1856T>G (HADHA)	ENSP00000493761.1:n.*1856T>G
ENST00000643063.1:c.*1011T>G (HADHA)	ENSP00000495353.1:n.*1011T>G
ENST00000643233.1:c.*1856T>G (HADHA)	ENSP00000493880.1:n.*1856T>G
ENST00000644428.1:c.*589T>G (HADHA)	ENSP00000495560.1:n.*589T>G
ENST00000645274.1:c.1860T>G (HADHA)	ENSP00000493996.1:p.Ile620Met
ENST00000646031.1:c.1324T>G (HADHA)
ENST00000646483.1:c.1831T>G (HADHA)	ENSP00000496185.1:n.1831T>G
ENST00000380649.7:c.1965T>G (HADHA)	ENSP00000370023.3:p.Ile655Met
ENST00000492433.1:c.423T>G (HADHA)	ENSP00000438039.1:p.Ile141Met
NM_000182.4:c.1965T>G (HADHA)	NP_000173.2:p.Ile655Met
XM_011532567.1:c.1683+5030A>C (GAREM2)	XP_011530869.1:n.1683+5030A>C
XM_011532567.3:c.1683+5030A>C (GAREM2)	XP_011530869.1:n.1683+5030A>C
NM_000182.5:c.1965T>G (HADHA) MANE Select	NP_000173.2:p.Ile655Met