Canonical Allele Identifier: CA1239705184
Gene: HADHA HGNC NCBI
GAREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26201186A= , CM000664.2:g.26201186A= GRCh38
NC_000002.11:g.26424055A= , CM000664.1:g.26424055A= GRCh37
NC_000002.10:g.26277559A= NCBI36
NG_007121.1:g.48435T=
NG_007121.2:g.48436T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380649.8:c.1355T= (HADHA) MANE Select ENSP00000370023.3:p.Leu452=
ENST00000492433.2:c.1355T= (HADHA) ENSP00000438039.2:p.Leu452=
ENST00000643057.1:c.*1246T= (HADHA) ENSP00000493761.1:n.*1246T=
ENST00000643063.1:c.*401T= (HADHA) ENSP00000495353.1:n.*401T=
ENST00000643233.1:c.*1246T= (HADHA) ENSP00000493880.1:n.*1246T=
ENST00000644428.1:c.1355T= (HADHA) ENSP00000495560.1:p.Leu452=
ENST00000645274.1:c.1250T= (HADHA) ENSP00000493996.1:p.Leu417=
ENST00000646031.1:c.714T= (HADHA)
ENST00000646483.1:c.1221T= (HADHA) ENSP00000496185.1:n.1221T=
ENST00000380649.7:c.1355T= (HADHA) ENSP00000370023.3:p.Leu452=
NM_000182.4:c.1355T= (HADHA) NP_000173.2:p.Leu452=
XM_011532567.1:c.1684-1047A= (GAREM2) XP_011530869.1:n.1684-1047A=
XM_011532567.3:c.1684-1047A= (GAREM2) XP_011530869.1:n.1684-1047A=
NM_000182.5:c.1355T= (HADHA) MANE Select NP_000173.2:p.Leu452=