Canonical Allele Identifier: CA1239702428

Gene: HADHA GAREM2

Linked Data

• dbSNP Id: rs1574603258

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26194859A>C , CM000664.2:g.26194859A>C	GRCh38
NC_000002.11:g.26417728A>C , CM000664.1:g.26417728A>C	GRCh37
NC_000002.10:g.26271232A>C	NCBI36
NG_007121.1:g.54762T>G
NG_007121.2:g.54763T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1621-221T>G (HADHA) MANE Select	ENSP00000370023.3:n.1621-221T>G
ENST00000492433.2:c.1621-221T>G (HADHA)	ENSP00000438039.2:n.1621-221T>G
ENST00000643057.1:c.*1512-221T>G (HADHA)	ENSP00000493761.1:n.*1512-221T>G
ENST00000643063.1:c.*667-221T>G (HADHA)	ENSP00000495353.1:n.*667-221T>G
ENST00000643233.1:c.*1512-221T>G (HADHA)	ENSP00000493880.1:n.*1512-221T>G
ENST00000644428.1:c.*245-221T>G (HADHA)	ENSP00000495560.1:n.*245-221T>G
ENST00000645274.1:c.1516-221T>G (HADHA)	ENSP00000493996.1:n.1516-221T>G
ENST00000646031.1:c.980-221T>G (HADHA)
ENST00000646483.1:c.1487-221T>G (HADHA)	ENSP00000496185.1:n.1487-221T>G
ENST00000380649.7:c.1621-221T>G (HADHA)	ENSP00000370023.3:n.1621-221T>G
ENST00000492433.1:c.79-221T>G (HADHA)	ENSP00000438039.1:n.79-221T>G
NM_000182.4:c.1621-221T>G (HADHA)	NP_000173.2:n.1621-221T>G
XM_011532567.1:c.1684-7374A>C (GAREM2)	XP_011530869.1:n.1684-7374A>C
XM_011532567.3:c.1684-7374A>C (GAREM2)	XP_011530869.1:n.1684-7374A>C
NM_000182.5:c.1621-221T>G (HADHA) MANE Select	NP_000173.2:n.1621-221T>G