Canonical Allele Identifier: CA425200624

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26417973G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26195104G>A , CM000664.2:g.26195104G>A	GRCh38
NC_000002.11:g.26417973G>A , CM000664.1:g.26417973G>A	GRCh37
NC_000002.10:g.26271477G>A	NCBI36
NG_007121.1:g.54517C>T
NG_007121.2:g.54518C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1608C>T (HADHA) MANE Select	ENSP00000370023.3:p.Ile536=
ENST00000492433.2:c.1608C>T (HADHA)	ENSP00000438039.2:p.Ile536=
ENST00000643057.1:c.*1499C>T (HADHA)	ENSP00000493761.1:n.*1499C>T
ENST00000643063.1:c.*654C>T (HADHA)	ENSP00000495353.1:n.*654C>T
ENST00000643233.1:c.*1499C>T (HADHA)	ENSP00000493880.1:n.*1499C>T
ENST00000644428.1:c.*232C>T (HADHA)	ENSP00000495560.1:n.*232C>T
ENST00000645274.1:c.1503C>T (HADHA)	ENSP00000493996.1:p.Ile501=
ENST00000646031.1:c.967C>T (HADHA)
ENST00000646483.1:c.1474C>T (HADHA)	ENSP00000496185.1:n.1474C>T
ENST00000380649.7:c.1608C>T (HADHA)	ENSP00000370023.3:p.Ile536=
ENST00000492433.1:c.66C>T (HADHA)	ENSP00000438039.1:p.Ile22=
NM_000182.4:c.1608C>T (HADHA)	NP_000173.2:p.Ile536=
XM_011532567.1:c.1684-7129G>A (GAREM2)	XP_011530869.1:n.1684-7129G>A
XM_011532567.3:c.1684-7129G>A (GAREM2)	XP_011530869.1:n.1684-7129G>A
NM_000182.5:c.1608C>T (HADHA) MANE Select	NP_000173.2:p.Ile536=