Canonical Allele Identifier: CA2740044069

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359655G>C , CM000685.2:g.19359655G>C	GRCh38
NC_000023.10:g.19377773G>C , CM000685.1:g.19377773G>C	GRCh37
NC_000023.9:g.19287694G>C	NCBI36
NG_016781.1:g.20763G>C
NG_021184.1:g.160607C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.*2G>C	ENSP00000348062.6:n.*2G>C
ENST00000379805.4:c.*867G>C	ENSP00000369133.3:n.*867G>C
ENST00000417819.6:c.*2G>C	ENSP00000404616.2:n.*2G>C
ENST00000423505.6:c.*2G>C	ENSP00000406473.2:n.*2G>C
ENST00000481733.2:n.970G>C
ENST00000696704.1:c.*507G>C	ENSP00000512823.1:n.*507G>C
ENST00000696705.1:c.*630G>C	ENSP00000512824.1:n.*630G>C
ENST00000422285.7:c.*2G>C MANE Select	ENSP00000394382.2:n.*2G>C
ENST00000379804.1:c.*2G>C	ENSP00000369132.1:n.*2G>C
ENST00000379806.9:c.*2G>C	ENSP00000369134.5:n.*2G>C
ENST00000422285.6:c.*2G>C	ENSP00000394382.2:n.*2G>C
ENST00000478795.1:n.614G>C
ENST00000540249.5:c.*2G>C	ENSP00000440761.1:n.*2G>C
ENST00000545074.5:c.*2G>C	ENSP00000438550.1:n.*2G>C
NM_000284.3:c.*2G>C	NP_000275.1:n.*2G>C
NM_001173454.1:c.*2G>C	NP_001166925.1:n.*2G>C
NM_001173455.1:c.*2G>C	NP_001166926.1:n.*2G>C
NM_001173456.1:c.*2G>C	NP_001166927.1:n.*2G>C
XM_011545531.1:c.*2G>C	XP_011543833.1:n.*2G>C
XM_011545532.1:c.*2G>C	XP_011543834.1:n.*2G>C
XM_017029574.2:c.*2G>C	XP_016885063.1:n.*2G>C
NM_000284.4:c.*2G>C MANE Select	NP_000275.1:n.*2G>C
NM_001173454.2:c.*2G>C	NP_001166925.1:n.*2G>C
NM_001173455.2:c.*2G>C	NP_001166926.1:n.*2G>C
NM_001173456.2:c.*2G>C	NP_001166927.1:n.*2G>C