Canonical Allele Identifier: CA425200106

Gene: HADHA GAREM2

Linked Data

• dbSNP Id: rs1157551585
• gnomAD v2: 2-26415250-C-G
• gnomAD v4: 2-26192381-C-G
• MyVariant Identifiers: chr2:g.26415250C>G (hg19) ; chr2:g.26192381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192381C>G , CM000664.2:g.26192381C>G	GRCh38
NC_000002.11:g.26415250C>G , CM000664.1:g.26415250C>G	GRCh37
NC_000002.10:g.26268754C>G	NCBI36
NG_007121.1:g.57240G>C
NG_007121.2:g.57241G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1929G>C (HADHA) MANE Select	ENSP00000370023.3:p.Val643=
ENST00000492433.2:c.1929G>C (HADHA)	ENSP00000438039.2:p.Val643=
ENST00000643057.1:c.*1820G>C (HADHA)	ENSP00000493761.1:n.*1820G>C
ENST00000643063.1:c.*975G>C (HADHA)	ENSP00000495353.1:n.*975G>C
ENST00000643233.1:c.*1820G>C (HADHA)	ENSP00000493880.1:n.*1820G>C
ENST00000644428.1:c.*553G>C (HADHA)	ENSP00000495560.1:n.*553G>C
ENST00000645274.1:c.1824G>C (HADHA)	ENSP00000493996.1:p.Val608=
ENST00000646031.1:c.1288G>C (HADHA)
ENST00000646483.1:c.1795G>C (HADHA)	ENSP00000496185.1:n.1795G>C
ENST00000380649.7:c.1929G>C (HADHA)	ENSP00000370023.3:p.Val643=
ENST00000492433.1:c.387G>C (HADHA)	ENSP00000438039.1:p.Val129=
NM_000182.4:c.1929G>C (HADHA)	NP_000173.2:p.Val643=
XM_011532567.1:c.1683+5066C>G (GAREM2)	XP_011530869.1:n.1683+5066C>G
XM_011532567.3:c.1683+5066C>G (GAREM2)	XP_011530869.1:n.1683+5066C>G
NM_000182.5:c.1929G>C (HADHA) MANE Select	NP_000173.2:p.Val643=