Canonical Allele Identifier: CA767267117

Gene: HADHA

Linked Data

• dbSNP Id: rs1420903046
• gnomAD v3: 2-26203899-C-T
• gnomAD v4: 2-26203899-C-T
• MyVariant Identifiers: chr2:g.26426768C>T (hg19) ; chr2:g.26203899C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26203899C>T , CM000664.2:g.26203899C>T	GRCh38
NC_000002.11:g.26426768C>T , CM000664.1:g.26426768C>T	GRCh37
NC_000002.10:g.26280272C>T	NCBI36
NG_007121.1:g.45722G>A
NG_007121.2:g.45723G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380649.8:c.1220+163G>A MANE Select	ENSP00000370023.3:n.1220+163G>A
ENST00000492433.2:c.1220+163G>A	ENSP00000438039.2:n.1220+163G>A
ENST00000643057.1:c.*1111+163G>A	ENSP00000493761.1:n.*1111+163G>A
ENST00000643063.1:c.*266+163G>A	ENSP00000495353.1:n.*266+163G>A
ENST00000643233.1:c.*1111+163G>A	ENSP00000493880.1:n.*1111+163G>A
ENST00000644428.1:c.1220+163G>A	ENSP00000495560.1:n.1220+163G>A
ENST00000645274.1:c.1115+163G>A	ENSP00000493996.1:n.1115+163G>A
ENST00000646031.1:c.579+163G>A
ENST00000646483.1:c.1086+163G>A	ENSP00000496185.1:n.1086+163G>A
ENST00000380649.7:c.1220+163G>A	ENSP00000370023.3:n.1220+163G>A
NM_000182.4:c.1220+163G>A	NP_000173.2:n.1220+163G>A
NM_000182.5:c.1220+163G>A MANE Select	NP_000173.2:n.1220+163G>A