Canonical Allele Identifier: CA346127220

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26424186C>A (hg19) ; chr2:g.26201317C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26201317C>A , CM000664.2:g.26201317C>A	GRCh38
NC_000002.11:g.26424186C>A , CM000664.1:g.26424186C>A	GRCh37
NC_000002.10:g.26277690C>A	NCBI36
NG_007121.1:g.48304G>T
NG_007121.2:g.48305G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1224G>T (HADHA) MANE Select	ENSP00000370023.3:p.Leu408Phe
ENST00000492433.2:c.1224G>T (HADHA)	ENSP00000438039.2:p.Leu408Phe
ENST00000643057.1:c.*1115G>T (HADHA)	ENSP00000493761.1:n.*1115G>T
ENST00000643063.1:c.*270G>T (HADHA)	ENSP00000495353.1:n.*270G>T
ENST00000643233.1:c.*1115G>T (HADHA)	ENSP00000493880.1:n.*1115G>T
ENST00000644428.1:c.1224G>T (HADHA)	ENSP00000495560.1:p.Leu408Phe
ENST00000645274.1:c.1119G>T (HADHA)	ENSP00000493996.1:p.Leu373Phe
ENST00000646031.1:c.583G>T (HADHA)
ENST00000646483.1:c.1090G>T (HADHA)	ENSP00000496185.1:n.1090G>T
ENST00000380649.7:c.1224G>T (HADHA)	ENSP00000370023.3:p.Leu408Phe
NM_000182.4:c.1224G>T (HADHA)	NP_000173.2:p.Leu408Phe
XM_011532567.1:c.1684-916C>A (GAREM2)	XP_011530869.1:n.1684-916C>A
XM_011532567.3:c.1684-916C>A (GAREM2)	XP_011530869.1:n.1684-916C>A
NM_000182.5:c.1224G>T (HADHA) MANE Select	NP_000173.2:p.Leu408Phe