Canonical Allele Identifier: CA2658210413

Gene: HADHA GAREM2

Linked Data

• gnomAD v4: 2-26192181-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192181G>A , CM000664.2:g.26192181G>A	GRCh38
NC_000002.11:g.26415050G>A , CM000664.1:g.26415050G>A	GRCh37
NC_000002.10:g.26268554G>A	NCBI36
NG_007121.1:g.57440C>T
NG_007121.2:g.57441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.2000+129C>T (HADHA) MANE Select	ENSP00000370023.3:n.2000+129C>T
ENST00000492433.2:c.2000+129C>T (HADHA)	ENSP00000438039.2:n.2000+129C>T
ENST00000643057.1:c.*1891+129C>T (HADHA)	ENSP00000493761.1:n.*1891+129C>T
ENST00000643063.1:c.*1046+129C>T (HADHA)	ENSP00000495353.1:n.*1046+129C>T
ENST00000643233.1:c.*1891+129C>T (HADHA)	ENSP00000493880.1:n.*1891+129C>T
ENST00000644428.1:c.*624+129C>T (HADHA)	ENSP00000495560.1:n.*624+129C>T
ENST00000645274.1:c.1895+129C>T (HADHA)	ENSP00000493996.1:n.1895+129C>T
ENST00000646031.1:c.1359+129C>T (HADHA)
ENST00000646483.1:c.1866+129C>T (HADHA)	ENSP00000496185.1:n.1866+129C>T
ENST00000380649.7:c.2000+129C>T (HADHA)	ENSP00000370023.3:n.2000+129C>T
ENST00000492433.1:c.458+129C>T (HADHA)	ENSP00000438039.1:n.458+129C>T
NM_000182.4:c.2000+129C>T (HADHA)	NP_000173.2:n.2000+129C>T
XM_011532567.1:c.1683+4866G>A (GAREM2)	XP_011530869.1:n.1683+4866G>A
XM_011532567.3:c.1683+4866G>A (GAREM2)	XP_011530869.1:n.1683+4866G>A
NM_000182.5:c.2000+129C>T (HADHA) MANE Select	NP_000173.2:n.2000+129C>T