Canonical Allele Identifier: CA346112372

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26414347C>G (hg19) ; chr2:g.26191478C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26191478C>G , CM000664.2:g.26191478C>G	GRCh38
NC_000002.11:g.26414347C>G , CM000664.1:g.26414347C>G	GRCh37
NC_000002.10:g.26267851C>G	NCBI36
NG_007121.1:g.58143G>C
NG_007121.2:g.58144G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2146+5G>C (HADHA) MANE Select	ENSP00000370023.3:n.2146+5G>C
ENST00000492433.2:c.2151G>C (HADHA)	ENSP00000438039.2:p.Trp717Cys
ENST00000643057.1:c.*2042G>C (HADHA)	ENSP00000493761.1:n.*2042G>C
ENST00000643063.1:c.*1192+5G>C (HADHA)	ENSP00000495353.1:n.*1192+5G>C
ENST00000643233.1:c.*2037+5G>C (HADHA)	ENSP00000493880.1:n.*2037+5G>C
ENST00000644428.1:c.*770+5G>C (HADHA)	ENSP00000495560.1:n.*770+5G>C
ENST00000645274.1:c.2041+5G>C (HADHA)	ENSP00000493996.1:n.2041+5G>C
ENST00000646031.1:c.1505+5G>C (HADHA)
ENST00000646483.1:c.2012+5G>C (HADHA)	ENSP00000496185.1:n.2012+5G>C
ENST00000380649.7:c.2146+5G>C (HADHA)	ENSP00000370023.3:n.2146+5G>C
ENST00000492433.1:c.609G>C (HADHA)	ENSP00000438039.1:p.Trp203Cys
NM_000182.4:c.2146+5G>C (HADHA)	NP_000173.2:n.2146+5G>C
XM_011532567.1:c.1683+4163C>G (GAREM2)	XP_011530869.1:n.1683+4163C>G
XM_011532567.3:c.1683+4163C>G (GAREM2)	XP_011530869.1:n.1683+4163C>G
NM_000182.5:c.2146+5G>C (HADHA) MANE Select	NP_000173.2:n.2146+5G>C