Canonical Allele Identifier: CA434040222

Gene: PDHB

Linked Data

• ClinVar Variation Id: 2756972
• ClinVar RCV Id: RCV003515152
• MyVariant Identifiers: chr3:g.58416490G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58430763G>A , CM000665.2:g.58430763G>A	GRCh38
NC_000003.11:g.58416490G>A , CM000665.1:g.58416490G>A	GRCh37
NC_000003.10:g.58391530G>A	NCBI36
NG_016860.1:g.8090C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.483C>T MANE Select	ENSP00000307241.6:p.Cys161=
ENST00000302746.10:c.483C>T	ENSP00000307241.6:p.Cys161=
ENST00000383714.8:c.429C>T	ENSP00000373220.4:p.Cys143=
ENST00000461692.5:n.596C>T
ENST00000469364.5:c.483C>T	ENSP00000419580.1:p.Cys161=
ENST00000474765.1:c.429C>T	ENSP00000418448.1:p.Cys143=
ENST00000479945.1:n.2888C>T
ENST00000480626.5:n.575C>T
ENST00000485460.5:c.429C>T	ENSP00000417267.1:p.Cys143=
NM_000925.3:c.483C>T	NP_000916.2:p.Cys161=
NM_001173468.1:c.429C>T	NP_001166939.1:p.Cys143=
NM_001315536.1:c.429C>T	NP_001302465.1:p.Cys143=
NR_033384.1:n.596C>T
NM_000925.4:c.483C>T MANE Select	NP_000916.2:p.Cys161=
NM_001173468.2:c.429C>T	NP_001166939.1:p.Cys143=
NM_001315536.2:c.429C>T	NP_001302465.1:p.Cys143=
NR_033384.2:n.589C>T