Canonical Allele Identifier: CA1239701220
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26192265_26192269delinsCAGAG , CM000664.2:g.26192265_26192269delinsCAGAG GRCh38
NC_000002.11:g.26415134_26415138delinsCAGAG , CM000664.1:g.26415134_26415138delinsCAGAG GRCh37
NC_000002.10:g.26268638_26268642delinsCAGAG NCBI36
NG_007121.1:g.57352_57356delinsCTCTG
NG_007121.2:g.57353_57357delinsCTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.2000+41_2000+45delinsCTCTG (HADHA) MANE Select ENSP00000370023.3:n.2000+41_2000+45delinsCTCTG
ENST00000492433.2:c.2000+41_2000+45delinsCTCTG (HADHA) ENSP00000438039.2:n.2000+41_2000+45delinsCTCTG
ENST00000643057.1:c.*1891+41_*1891+45delinsCTCTG (HADHA) ENSP00000493761.1:n.*1891+41_*1891+45delinsCTCTG
ENST00000643063.1:c.*1046+41_*1046+45delinsCTCTG (HADHA) ENSP00000495353.1:n.*1046+41_*1046+45delinsCTCTG
ENST00000643233.1:c.*1891+41_*1891+45delinsCTCTG (HADHA) ENSP00000493880.1:n.*1891+41_*1891+45delinsCTCTG
ENST00000644428.1:c.*624+41_*624+45delinsCTCTG (HADHA) ENSP00000495560.1:n.*624+41_*624+45delinsCTCTG
ENST00000645274.1:c.1895+41_1895+45delinsCTCTG (HADHA) ENSP00000493996.1:n.1895+41_1895+45delinsCTCTG
ENST00000646031.1:c.1359+41_1359+45delinsCTCTG (HADHA)
ENST00000646483.1:c.1866+41_1866+45delinsCTCTG (HADHA) ENSP00000496185.1:n.1866+41_1866+45delinsCTCTG
ENST00000380649.7:c.2000+41_2000+45delinsCTCTG (HADHA) ENSP00000370023.3:n.2000+41_2000+45delinsCTCTG
ENST00000492433.1:c.458+41_458+45delinsCTCTG (HADHA) ENSP00000438039.1:n.458+41_458+45delinsCTCTG
NM_000182.4:c.2000+41_2000+45delinsCTCTG (HADHA) NP_000173.2:n.2000+41_2000+45delinsCTCTG
XM_011532567.1:c.1683+4950_1683+4954delinsCAGAG (GAREM2) XP_011530869.1:n.1683+4950_1683+4954delinsCAGAG
XM_011532567.3:c.1683+4950_1683+4954delinsCAGAG (GAREM2) XP_011530869.1:n.1683+4950_1683+4954delinsCAGAG
NM_000182.5:c.2000+41_2000+45delinsCTCTG (HADHA) MANE Select NP_000173.2:n.2000+41_2000+45delinsCTCTG