Canonical Allele Identifier: CA425200093

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26415220A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192351A>G , CM000664.2:g.26192351A>G	GRCh38
NC_000002.11:g.26415220A>G , CM000664.1:g.26415220A>G	GRCh37
NC_000002.10:g.26268724A>G	NCBI36
NG_007121.1:g.57270T>C
NG_007121.2:g.57271T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.1959T>C (HADHA) MANE Select	ENSP00000370023.3:p.Asp653=
ENST00000492433.2:c.1959T>C (HADHA)	ENSP00000438039.2:p.Asp653=
ENST00000643057.1:c.*1850T>C (HADHA)	ENSP00000493761.1:n.*1850T>C
ENST00000643063.1:c.*1005T>C (HADHA)	ENSP00000495353.1:n.*1005T>C
ENST00000643233.1:c.*1850T>C (HADHA)	ENSP00000493880.1:n.*1850T>C
ENST00000644428.1:c.*583T>C (HADHA)	ENSP00000495560.1:n.*583T>C
ENST00000645274.1:c.1854T>C (HADHA)	ENSP00000493996.1:p.Asp618=
ENST00000646031.1:c.1318T>C (HADHA)
ENST00000646483.1:c.1825T>C (HADHA)	ENSP00000496185.1:n.1825T>C
ENST00000380649.7:c.1959T>C (HADHA)	ENSP00000370023.3:p.Asp653=
ENST00000492433.1:c.417T>C (HADHA)	ENSP00000438039.1:p.Asp139=
NM_000182.4:c.1959T>C (HADHA)	NP_000173.2:p.Asp653=
XM_011532567.1:c.1683+5036A>G (GAREM2)	XP_011530869.1:n.1683+5036A>G
XM_011532567.3:c.1683+5036A>G (GAREM2)	XP_011530869.1:n.1683+5036A>G
NM_000182.5:c.1959T>C (HADHA) MANE Select	NP_000173.2:p.Asp653=