Canonical Allele Identifier: CA346115649

Gene: HADHA GAREM2

Linked Data

• ClinVar Variation Id: 1726289
• ClinVar RCV Id: RCV002307260
• MyVariant Identifiers: chr2:g.26415288T>A (hg19) ; chr2:g.26192419T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192419T>A , CM000664.2:g.26192419T>A	GRCh38
NC_000002.11:g.26415288T>A , CM000664.1:g.26415288T>A	GRCh37
NC_000002.10:g.26268792T>A	NCBI36
NG_007121.1:g.57202A>T
NG_007121.2:g.57203A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1891A>T (HADHA) MANE Select	ENSP00000370023.3:p.Lys631Ter
ENST00000492433.2:c.1891A>T (HADHA)	ENSP00000438039.2:p.Lys631Ter
ENST00000643057.1:c.*1782A>T (HADHA)	ENSP00000493761.1:n.*1782A>T
ENST00000643063.1:c.*937A>T (HADHA)	ENSP00000495353.1:n.*937A>T
ENST00000643233.1:c.*1782A>T (HADHA)	ENSP00000493880.1:n.*1782A>T
ENST00000644428.1:c.*515A>T (HADHA)	ENSP00000495560.1:n.*515A>T
ENST00000645274.1:c.1786A>T (HADHA)	ENSP00000493996.1:p.Lys596Ter
ENST00000646031.1:c.1250A>T (HADHA)
ENST00000646483.1:c.1757A>T (HADHA)	ENSP00000496185.1:n.1757A>T
ENST00000380649.7:c.1891A>T (HADHA)	ENSP00000370023.3:p.Lys631Ter
ENST00000492433.1:c.349A>T (HADHA)	ENSP00000438039.1:p.Lys117Ter
NM_000182.4:c.1891A>T (HADHA)	NP_000173.2:p.Lys631Ter
XM_011532567.1:c.1683+5104T>A (GAREM2)	XP_011530869.1:n.1683+5104T>A
XM_011532567.3:c.1683+5104T>A (GAREM2)	XP_011530869.1:n.1683+5104T>A
NM_000182.5:c.1891A>T (HADHA) MANE Select	NP_000173.2:p.Lys631Ter