Canonical Allele Identifier: CA1367631329

Gene: PDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58430820T= , CM000665.2:g.58430820T=	GRCh38
NC_000003.11:g.58416547T= , CM000665.1:g.58416547T=	GRCh37
NC_000003.10:g.58391587T=	NCBI36
NG_016860.1:g.8033A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.426A= MANE Select	ENSP00000307241.6:p.Ile142=
ENST00000302746.10:c.426A=	ENSP00000307241.6:p.Ile142=
ENST00000383714.8:c.372A=	ENSP00000373220.4:p.Ile124=
ENST00000461692.5:n.539A=
ENST00000469364.5:c.426A=	ENSP00000419580.1:p.Ile142=
ENST00000474765.1:c.372A=	ENSP00000418448.1:p.Ile124=
ENST00000479945.1:n.2831A=
ENST00000480626.5:n.518A=
ENST00000485460.5:c.403+23A=	ENSP00000417267.1:n.403+23A=
NM_000925.3:c.426A=	NP_000916.2:p.Ile142=
NM_001173468.1:c.403+23A=	NP_001166939.1:n.403+23A=
NM_001315536.1:c.372A=	NP_001302465.1:p.Ile124=
NR_033384.1:n.539A=
NM_000925.4:c.426A= MANE Select	NP_000916.2:p.Ile142=
NM_001173468.2:c.403+23A=	NP_001166939.1:n.403+23A=
NM_001315536.2:c.372A=	NP_001302465.1:p.Ile124=
NR_033384.2:n.532A=