Canonical Allele Identifier: CA346128867

Gene: HADHA

Linked Data

• MyVariant Identifiers: chr2:g.26426965C>A (hg19) ; chr2:g.26204096C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204096C>A , CM000664.2:g.26204096C>A	GRCh38
NC_000002.11:g.26426965C>A , CM000664.1:g.26426965C>A	GRCh37
NC_000002.10:g.26280469C>A	NCBI36
NG_007121.1:g.45525G>T
NG_007121.2:g.45526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1186G>T MANE Select	ENSP00000370023.3:p.Ala396Ser
ENST00000492433.2:c.1186G>T	ENSP00000438039.2:p.Ala396Ser
ENST00000643057.1:c.*1077G>T	ENSP00000493761.1:n.*1077G>T
ENST00000643063.1:c.*232G>T	ENSP00000495353.1:n.*232G>T
ENST00000643233.1:c.*1077G>T	ENSP00000493880.1:n.*1077G>T
ENST00000644428.1:c.1186G>T	ENSP00000495560.1:p.Ala396Ser
ENST00000645274.1:c.1081G>T	ENSP00000493996.1:p.Ala361Ser
ENST00000646031.1:c.545G>T
ENST00000646483.1:c.1052G>T	ENSP00000496185.1:n.1052G>T
ENST00000380649.7:c.1186G>T	ENSP00000370023.3:p.Ala396Ser
NM_000182.4:c.1186G>T	NP_000173.2:p.Ala396Ser
NM_000182.5:c.1186G>T MANE Select	NP_000173.2:p.Ala396Ser