Canonical Allele Identifier: CA425200080

Gene: HADHA GAREM2

Linked Data

• gnomAD v4: 2-26192330-C-T
• MyVariant Identifiers: chr2:g.26415199C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192330C>T , CM000664.2:g.26192330C>T	GRCh38
NC_000002.11:g.26415199C>T , CM000664.1:g.26415199C>T	GRCh37
NC_000002.10:g.26268703C>T	NCBI36
NG_007121.1:g.57291G>A
NG_007121.2:g.57292G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1980G>A (HADHA) MANE Select	ENSP00000370023.3:p.Lys660=
ENST00000492433.2:c.1980G>A (HADHA)	ENSP00000438039.2:p.Lys660=
ENST00000643057.1:c.*1871G>A (HADHA)	ENSP00000493761.1:n.*1871G>A
ENST00000643063.1:c.*1026G>A (HADHA)	ENSP00000495353.1:n.*1026G>A
ENST00000643233.1:c.*1871G>A (HADHA)	ENSP00000493880.1:n.*1871G>A
ENST00000644428.1:c.*604G>A (HADHA)	ENSP00000495560.1:n.*604G>A
ENST00000645274.1:c.1875G>A (HADHA)	ENSP00000493996.1:p.Lys625=
ENST00000646031.1:c.1339G>A (HADHA)
ENST00000646483.1:c.1846G>A (HADHA)	ENSP00000496185.1:n.1846G>A
ENST00000380649.7:c.1980G>A (HADHA)	ENSP00000370023.3:p.Lys660=
ENST00000492433.1:c.438G>A (HADHA)	ENSP00000438039.1:p.Lys146=
NM_000182.4:c.1980G>A (HADHA)	NP_000173.2:p.Lys660=
XM_011532567.1:c.1683+5015C>T (GAREM2)	XP_011530869.1:n.1683+5015C>T
XM_011532567.3:c.1683+5015C>T (GAREM2)	XP_011530869.1:n.1683+5015C>T
NM_000182.5:c.1980G>A (HADHA) MANE Select	NP_000173.2:p.Lys660=