Canonical Allele Identifier: CA353362888

Gene: PDHB

Linked Data

• MyVariant Identifiers: chr3:g.58417322T>A (hg19) ; chr3:g.58431595T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58431595T>A , CM000665.2:g.58431595T>A	GRCh38
NC_000003.11:g.58417322T>A , CM000665.1:g.58417322T>A	GRCh37
NC_000003.10:g.58392362T>A	NCBI36
NG_016860.1:g.7258A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302746.11:c.301A>T MANE Select	ENSP00000307241.6:p.Met101Leu
ENST00000302746.10:c.301A>T	ENSP00000307241.6:p.Met101Leu
ENST00000383714.8:c.247A>T	ENSP00000373220.4:p.Met83Leu
ENST00000461692.5:n.414A>T
ENST00000469364.5:c.301A>T	ENSP00000419580.1:p.Met101Leu
ENST00000469827.1:n.423A>T
ENST00000474765.1:c.247A>T	ENSP00000418448.1:p.Met83Leu
ENST00000479945.1:n.2056A>T
ENST00000480626.5:n.393A>T
ENST00000482894.5:n.320A>T
ENST00000485460.5:c.301A>T	ENSP00000417267.1:p.Met101Leu
NM_000925.3:c.301A>T	NP_000916.2:p.Met101Leu
NM_001173468.1:c.301A>T	NP_001166939.1:p.Met101Leu
NM_001315536.1:c.247A>T	NP_001302465.1:p.Met83Leu
NR_033384.1:n.414A>T
NM_000925.4:c.301A>T MANE Select	NP_000916.2:p.Met101Leu
NM_001173468.2:c.301A>T	NP_001166939.1:p.Met101Leu
NM_001315536.2:c.247A>T	NP_001302465.1:p.Met83Leu
NR_033384.2:n.407A>T