Canonical Allele Identifier: CA346126465

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26424055A>T (hg19) ; chr2:g.26201186A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1355T>A (HADHA) MANE Select	ENSP00000370023.3:p.Leu452His
ENST00000492433.2:c.1355T>A (HADHA)	ENSP00000438039.2:p.Leu452His
ENST00000643057.1:c.*1246T>A (HADHA)	ENSP00000493761.1:n.*1246T>A
ENST00000643063.1:c.*401T>A (HADHA)	ENSP00000495353.1:n.*401T>A
ENST00000643233.1:c.*1246T>A (HADHA)	ENSP00000493880.1:n.*1246T>A
ENST00000644428.1:c.1355T>A (HADHA)	ENSP00000495560.1:p.Leu452His
ENST00000645274.1:c.1250T>A (HADHA)	ENSP00000493996.1:p.Leu417His
ENST00000646031.1:c.714T>A (HADHA)
ENST00000646483.1:c.1221T>A (HADHA)	ENSP00000496185.1:n.1221T>A
ENST00000380649.7:c.1355T>A (HADHA)	ENSP00000370023.3:p.Leu452His
NM_000182.4:c.1355T>A (HADHA)	NP_000173.2:p.Leu452His
XM_011532567.1:c.1684-1047A>T (GAREM2)	XP_011530869.1:n.1684-1047A>T
XM_011532567.3:c.1684-1047A>T (GAREM2)	XP_011530869.1:n.1684-1047A>T
NM_000182.5:c.1355T>A (HADHA) MANE Select	NP_000173.2:p.Leu452His