Canonical Allele Identifier: CA434040651

Gene: PDHB

Linked Data

• MyVariant Identifiers: chr3:g.58417326T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58431599T>A , CM000665.2:g.58431599T>A	GRCh38
NC_000003.11:g.58417326T>A , CM000665.1:g.58417326T>A	GRCh37
NC_000003.10:g.58392366T>A	NCBI36
NG_016860.1:g.7254A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.297A>T MANE Select	ENSP00000307241.6:p.Ala99=
ENST00000302746.10:c.297A>T	ENSP00000307241.6:p.Ala99=
ENST00000383714.8:c.243A>T	ENSP00000373220.4:p.Ala81=
ENST00000461692.5:n.410A>T
ENST00000469364.5:c.297A>T	ENSP00000419580.1:p.Ala99=
ENST00000469827.1:n.419A>T
ENST00000474765.1:c.243A>T	ENSP00000418448.1:p.Ala81=
ENST00000479945.1:n.2052A>T
ENST00000480626.5:n.389A>T
ENST00000482894.5:n.316A>T
ENST00000485460.5:c.297A>T	ENSP00000417267.1:p.Ala99=
NM_000925.3:c.297A>T	NP_000916.2:p.Ala99=
NM_001173468.1:c.297A>T	NP_001166939.1:p.Ala99=
NM_001315536.1:c.243A>T	NP_001302465.1:p.Ala81=
NR_033384.1:n.410A>T
NM_000925.4:c.297A>T MANE Select	NP_000916.2:p.Ala99=
NM_001173468.2:c.297A>T	NP_001166939.1:p.Ala99=
NM_001315536.2:c.243A>T	NP_001302465.1:p.Ala81=
NR_033384.2:n.403A>T