Canonical Allele Identifier: CA1367631333

Gene: PDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58430827A= , CM000665.2:g.58430827A=	GRCh38
NC_000003.11:g.58416554A= , CM000665.1:g.58416554A=	GRCh37
NC_000003.10:g.58391594A=	NCBI36
NG_016860.1:g.8026T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.419T= MANE Select	ENSP00000307241.6:p.Val140=
ENST00000302746.10:c.419T=	ENSP00000307241.6:p.Val140=
ENST00000383714.8:c.365T=	ENSP00000373220.4:p.Val122=
ENST00000461692.5:n.532T=
ENST00000469364.5:c.419T=	ENSP00000419580.1:p.Val140=
ENST00000474765.1:c.365T=	ENSP00000418448.1:p.Val122=
ENST00000479945.1:n.2824T=
ENST00000480626.5:n.511T=
ENST00000485460.5:c.403+16T=	ENSP00000417267.1:n.403+16T=
NM_000925.3:c.419T=	NP_000916.2:p.Val140=
NM_001173468.1:c.403+16T=	NP_001166939.1:n.403+16T=
NM_001315536.1:c.365T=	NP_001302465.1:p.Val122=
NR_033384.1:n.532T=
NM_000925.4:c.419T= MANE Select	NP_000916.2:p.Val140=
NM_001173468.2:c.403+16T=	NP_001166939.1:n.403+16T=
NM_001315536.2:c.365T=	NP_001302465.1:p.Val122=
NR_033384.2:n.525T=