Canonical Allele Identifier: CA346114460

Gene: HADHA GAREM2

Linked Data

• gnomAD v4: 2-26192335-G-T
• MyVariant Identifiers: chr2:g.26415204G>T (hg19) ; chr2:g.26192335G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192335G>T , CM000664.2:g.26192335G>T	GRCh38
NC_000002.11:g.26415204G>T , CM000664.1:g.26415204G>T	GRCh37
NC_000002.10:g.26268708G>T	NCBI36
NG_007121.1:g.57286C>A
NG_007121.2:g.57287C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1975C>A (HADHA) MANE Select	ENSP00000370023.3:p.Leu659Met
ENST00000492433.2:c.1975C>A (HADHA)	ENSP00000438039.2:p.Leu659Met
ENST00000643057.1:c.*1866C>A (HADHA)	ENSP00000493761.1:n.*1866C>A
ENST00000643063.1:c.*1021C>A (HADHA)	ENSP00000495353.1:n.*1021C>A
ENST00000643233.1:c.*1866C>A (HADHA)	ENSP00000493880.1:n.*1866C>A
ENST00000644428.1:c.*599C>A (HADHA)	ENSP00000495560.1:n.*599C>A
ENST00000645274.1:c.1870C>A (HADHA)	ENSP00000493996.1:p.Leu624Met
ENST00000646031.1:c.1334C>A (HADHA)
ENST00000646483.1:c.1841C>A (HADHA)	ENSP00000496185.1:n.1841C>A
ENST00000380649.7:c.1975C>A (HADHA)	ENSP00000370023.3:p.Leu659Met
ENST00000492433.1:c.433C>A (HADHA)	ENSP00000438039.1:p.Leu145Met
NM_000182.4:c.1975C>A (HADHA)	NP_000173.2:p.Leu659Met
XM_011532567.1:c.1683+5020G>T (GAREM2)	XP_011530869.1:n.1683+5020G>T
XM_011532567.3:c.1683+5020G>T (GAREM2)	XP_011530869.1:n.1683+5020G>T
NM_000182.5:c.1975C>A (HADHA) MANE Select	NP_000173.2:p.Leu659Met