Canonical Allele Identifier: CA2576696712

Gene: HADHA GAREM2

Linked Data

• gnomAD v4: 2-26195051-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26195051A>G , CM000664.2:g.26195051A>G	GRCh38
NC_000002.11:g.26417920A>G , CM000664.1:g.26417920A>G	GRCh37
NC_000002.10:g.26271424A>G	NCBI36
NG_007121.1:g.54570T>C
NG_007121.2:g.54571T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1620+41T>C (HADHA) MANE Select	ENSP00000370023.3:n.1620+41T>C
ENST00000492433.2:c.1620+41T>C (HADHA)	ENSP00000438039.2:n.1620+41T>C
ENST00000643057.1:c.*1511+41T>C (HADHA)	ENSP00000493761.1:n.*1511+41T>C
ENST00000643063.1:c.*666+41T>C (HADHA)	ENSP00000495353.1:n.*666+41T>C
ENST00000643233.1:c.*1511+41T>C (HADHA)	ENSP00000493880.1:n.*1511+41T>C
ENST00000644428.1:c.*244+41T>C (HADHA)	ENSP00000495560.1:n.*244+41T>C
ENST00000645274.1:c.1515+41T>C (HADHA)	ENSP00000493996.1:n.1515+41T>C
ENST00000646031.1:c.979+41T>C (HADHA)
ENST00000646483.1:c.1486+41T>C (HADHA)	ENSP00000496185.1:n.1486+41T>C
ENST00000380649.7:c.1620+41T>C (HADHA)	ENSP00000370023.3:n.1620+41T>C
ENST00000492433.1:c.78+41T>C (HADHA)	ENSP00000438039.1:n.78+41T>C
NM_000182.4:c.1620+41T>C (HADHA)	NP_000173.2:n.1620+41T>C
XM_011532567.1:c.1684-7182A>G (GAREM2)	XP_011530869.1:n.1684-7182A>G
XM_011532567.3:c.1684-7182A>G (GAREM2)	XP_011530869.1:n.1684-7182A>G
NM_000182.5:c.1620+41T>C (HADHA) MANE Select	NP_000173.2:n.1620+41T>C