Canonical Allele Identifier: CA346114204

Gene: HADHA GAREM2

Linked Data

• MyVariant Identifiers: chr2:g.26415180C>A (hg19) ; chr2:g.26192311C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192311C>A , CM000664.2:g.26192311C>A	GRCh38
NC_000002.11:g.26415180C>A , CM000664.1:g.26415180C>A	GRCh37
NC_000002.10:g.26268684C>A	NCBI36
NG_007121.1:g.57310G>T
NG_007121.2:g.57311G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.1999G>T (HADHA) MANE Select	ENSP00000370023.3:p.Val667Phe
ENST00000492433.2:c.1999G>T (HADHA)	ENSP00000438039.2:p.Val667Phe
ENST00000643057.1:c.*1890G>T (HADHA)	ENSP00000493761.1:n.*1890G>T
ENST00000643063.1:c.*1045G>T (HADHA)	ENSP00000495353.1:n.*1045G>T
ENST00000643233.1:c.*1890G>T (HADHA)	ENSP00000493880.1:n.*1890G>T
ENST00000644428.1:c.*623G>T (HADHA)	ENSP00000495560.1:n.*623G>T
ENST00000645274.1:c.1894G>T (HADHA)	ENSP00000493996.1:p.Val632Phe
ENST00000646031.1:c.1358G>T (HADHA)
ENST00000646483.1:c.1865G>T (HADHA)	ENSP00000496185.1:n.1865G>T
ENST00000380649.7:c.1999G>T (HADHA)	ENSP00000370023.3:p.Val667Phe
ENST00000492433.1:c.457G>T (HADHA)	ENSP00000438039.1:p.Val153Phe
NM_000182.4:c.1999G>T (HADHA)	NP_000173.2:p.Val667Phe
XM_011532567.1:c.1683+4996C>A (GAREM2)	XP_011530869.1:n.1683+4996C>A
XM_011532567.3:c.1683+4996C>A (GAREM2)	XP_011530869.1:n.1683+4996C>A
NM_000182.5:c.1999G>T (HADHA) MANE Select	NP_000173.2:p.Val667Phe