Canonical Allele Identifier: CA353362869

Gene: PDHB

Linked Data

• MyVariant Identifiers: chr3:g.58417318A>T (hg19) ; chr3:g.58431591A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58431591A>T , CM000665.2:g.58431591A>T	GRCh38
NC_000003.11:g.58417318A>T , CM000665.1:g.58417318A>T	GRCh37
NC_000003.10:g.58392358A>T	NCBI36
NG_016860.1:g.7262T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000302746.11:c.303+2T>A MANE Select	ENSP00000307241.6:n.303+2T>A
ENST00000302746.10:c.303+2T>A	ENSP00000307241.6:n.303+2T>A
ENST00000383714.8:c.249+2T>A	ENSP00000373220.4:n.249+2T>A
ENST00000461692.5:n.416+2T>A
ENST00000469364.5:c.303+2T>A	ENSP00000419580.1:n.303+2T>A
ENST00000469827.1:n.427T>A
ENST00000474765.1:c.249+2T>A	ENSP00000418448.1:n.249+2T>A
ENST00000479945.1:n.2060T>A
ENST00000480626.5:n.395+2T>A
ENST00000482894.5:n.324T>A
ENST00000485460.5:c.303+2T>A	ENSP00000417267.1:n.303+2T>A
NM_000925.3:c.303+2T>A	NP_000916.2:n.303+2T>A
NM_001173468.1:c.303+2T>A	NP_001166939.1:n.303+2T>A
NM_001315536.1:c.249+2T>A	NP_001302465.1:n.249+2T>A
NR_033384.1:n.416+2T>A
NM_000925.4:c.303+2T>A MANE Select	NP_000916.2:n.303+2T>A
NM_001173468.2:c.303+2T>A	NP_001166939.1:n.303+2T>A
NM_001315536.2:c.249+2T>A	NP_001302465.1:n.249+2T>A
NR_033384.2:n.409+2T>A