Canonical Allele Identifier: CA425357820

Gene: HADHA GAREM2

Linked Data

• gnomAD v4: 2-26191292-T-C
• MyVariant Identifiers: chr2:g.26414161T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191292T>C , CM000664.2:g.26191292T>C	GRCh38
NC_000002.11:g.26414161T>C , CM000664.1:g.26414161T>C	GRCh37
NC_000002.10:g.26267665T>C	NCBI36
NG_007121.1:g.58329A>G
NG_007121.2:g.58330A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2250A>G (HADHA) MANE Select	ENSP00000370023.3:p.Leu750=
ENST00000492433.2:c.2337A>G (HADHA)	ENSP00000438039.2:p.Leu779=
ENST00000643057.1:c.*2228A>G (HADHA)	ENSP00000493761.1:n.*2228A>G
ENST00000643063.1:c.*1296A>G (HADHA)	ENSP00000495353.1:n.*1296A>G
ENST00000643233.1:c.*2141A>G (HADHA)	ENSP00000493880.1:n.*2141A>G
ENST00000644428.1:c.*874A>G (HADHA)	ENSP00000495560.1:n.*874A>G
ENST00000645274.1:c.2145A>G (HADHA)	ENSP00000493996.1:p.Leu715=
ENST00000646031.1:c.1609A>G (HADHA)
ENST00000646483.1:c.2116A>G (HADHA)	ENSP00000496185.1:n.2116A>G
ENST00000380649.7:c.2250A>G (HADHA)	ENSP00000370023.3:p.Leu750=
NM_000182.4:c.2250A>G (HADHA)	NP_000173.2:p.Leu750=
XM_011532567.1:c.1683+3977T>C (GAREM2)	XP_011530869.1:n.1683+3977T>C
XM_011532567.3:c.1683+3977T>C (GAREM2)	XP_011530869.1:n.1683+3977T>C
NM_000182.5:c.2250A>G (HADHA) MANE Select	NP_000173.2:p.Leu750=