Canonical Allele Identifier: CA353361329

Gene: PDHB

Linked Data

• ClinVar Variation Id: 2799883
• ClinVar RCV Id: RCV003627667
• MyVariant Identifiers: chr3:g.58416478C>T (hg19) ; chr3:g.58430751C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58430751C>T , CM000665.2:g.58430751C>T	GRCh38
NC_000003.11:g.58416478C>T , CM000665.1:g.58416478C>T	GRCh37
NC_000003.10:g.58391518C>T	NCBI36
NG_016860.1:g.8102G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.495G>A MANE Select	ENSP00000307241.6:p.Trp165Ter
ENST00000302746.10:c.495G>A	ENSP00000307241.6:p.Trp165Ter
ENST00000383714.8:c.441G>A	ENSP00000373220.4:p.Trp147Ter
ENST00000461692.5:n.608G>A
ENST00000469364.5:c.495G>A	ENSP00000419580.1:p.Trp165Ter
ENST00000474765.1:c.441G>A	ENSP00000418448.1:p.Trp147Ter
ENST00000479945.1:n.2900G>A
ENST00000480626.5:n.587G>A
ENST00000485460.5:c.441G>A	ENSP00000417267.1:p.Trp147Ter
NM_000925.3:c.495G>A	NP_000916.2:p.Trp165Ter
NM_001173468.1:c.441G>A	NP_001166939.1:p.Trp147Ter
NM_001315536.1:c.441G>A	NP_001302465.1:p.Trp147Ter
NR_033384.1:n.608G>A
NM_000925.4:c.495G>A MANE Select	NP_000916.2:p.Trp165Ter
NM_001173468.2:c.441G>A	NP_001166939.1:p.Trp147Ter
NM_001315536.2:c.441G>A	NP_001302465.1:p.Trp147Ter
NR_033384.2:n.601G>A