Canonical Allele Identifier: CA44386039

Gene: HADHA

Linked Data

• dbSNP Id: rs112596398
• gnomAD v3: 2-26203953-G-A
• gnomAD v4: 2-26203953-G-A
• MyVariant Identifiers: chr2:g.26426822G>A (hg19) ; chr2:g.26203953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26203953G>A , CM000664.2:g.26203953G>A	GRCh38
NC_000002.11:g.26426822G>A , CM000664.1:g.26426822G>A	GRCh37
NC_000002.10:g.26280326G>A	NCBI36
NG_007121.1:g.45668C>T
NG_007121.2:g.45669C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1220+109C>T MANE Select	ENSP00000370023.3:n.1220+109C>T
ENST00000492433.2:c.1220+109C>T	ENSP00000438039.2:n.1220+109C>T
ENST00000643057.1:c.*1111+109C>T	ENSP00000493761.1:n.*1111+109C>T
ENST00000643063.1:c.*266+109C>T	ENSP00000495353.1:n.*266+109C>T
ENST00000643233.1:c.*1111+109C>T	ENSP00000493880.1:n.*1111+109C>T
ENST00000644428.1:c.1220+109C>T	ENSP00000495560.1:n.1220+109C>T
ENST00000645274.1:c.1115+109C>T	ENSP00000493996.1:n.1115+109C>T
ENST00000646031.1:c.579+109C>T
ENST00000646483.1:c.1086+109C>T	ENSP00000496185.1:n.1086+109C>T
ENST00000380649.7:c.1220+109C>T	ENSP00000370023.3:n.1220+109C>T
NM_000182.4:c.1220+109C>T	NP_000173.2:n.1220+109C>T
NM_000182.5:c.1220+109C>T MANE Select	NP_000173.2:n.1220+109C>T