Canonical Allele Identifier: CA353362905

Gene: PDHB

Linked Data

• gnomAD v4: 3-58431600-G-A
• MyVariant Identifiers: chr3:g.58417327G>A (hg19) ; chr3:g.58431600G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58431600G>A , CM000665.2:g.58431600G>A	GRCh38
NC_000003.11:g.58417327G>A , CM000665.1:g.58417327G>A	GRCh37
NC_000003.10:g.58392367G>A	NCBI36
NG_016860.1:g.7253C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.296C>T MANE Select	ENSP00000307241.6:p.Ala99Val
ENST00000302746.10:c.296C>T	ENSP00000307241.6:p.Ala99Val
ENST00000383714.8:c.242C>T	ENSP00000373220.4:p.Ala81Val
ENST00000461692.5:n.409C>T
ENST00000469364.5:c.296C>T	ENSP00000419580.1:p.Ala99Val
ENST00000469827.1:n.418C>T
ENST00000474765.1:c.242C>T	ENSP00000418448.1:p.Ala81Val
ENST00000479945.1:n.2051C>T
ENST00000480626.5:n.388C>T
ENST00000482894.5:n.315C>T
ENST00000485460.5:c.296C>T	ENSP00000417267.1:p.Ala99Val
NM_000925.3:c.296C>T	NP_000916.2:p.Ala99Val
NM_001173468.1:c.296C>T	NP_001166939.1:p.Ala99Val
NM_001315536.1:c.242C>T	NP_001302465.1:p.Ala81Val
NR_033384.1:n.409C>T
NM_000925.4:c.296C>T MANE Select	NP_000916.2:p.Ala99Val
NM_001173468.2:c.296C>T	NP_001166939.1:p.Ala99Val
NM_001315536.2:c.242C>T	NP_001302465.1:p.Ala81Val
NR_033384.2:n.402C>T