Canonical Allele Identifier: CA353361971

Gene: PDHB

Linked Data

• MyVariant Identifiers: chr3:g.58416551G>C (hg19) ; chr3:g.58430824G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58430824G>C , CM000665.2:g.58430824G>C	GRCh38
NC_000003.11:g.58416551G>C , CM000665.1:g.58416551G>C	GRCh37
NC_000003.10:g.58391591G>C	NCBI36
NG_016860.1:g.8029C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.422C>G MANE Select	ENSP00000307241.6:p.Pro141Arg
ENST00000302746.10:c.422C>G	ENSP00000307241.6:p.Pro141Arg
ENST00000383714.8:c.368C>G	ENSP00000373220.4:p.Pro123Arg
ENST00000461692.5:n.535C>G
ENST00000469364.5:c.422C>G	ENSP00000419580.1:p.Pro141Arg
ENST00000474765.1:c.368C>G	ENSP00000418448.1:p.Pro123Arg
ENST00000479945.1:n.2827C>G
ENST00000480626.5:n.514C>G
ENST00000485460.5:c.403+19C>G	ENSP00000417267.1:n.403+19C>G
NM_000925.3:c.422C>G	NP_000916.2:p.Pro141Arg
NM_001173468.1:c.403+19C>G	NP_001166939.1:n.403+19C>G
NM_001315536.1:c.368C>G	NP_001302465.1:p.Pro123Arg
NR_033384.1:n.535C>G
NM_000925.4:c.422C>G MANE Select	NP_000916.2:p.Pro141Arg
NM_001173468.2:c.403+19C>G	NP_001166939.1:n.403+19C>G
NM_001315536.2:c.368C>G	NP_001302465.1:p.Pro123Arg
NR_033384.2:n.528C>G