Canonical Allele Identifier: CA2418222741

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19352978_19352980delinsCTG , CM000685.2:g.19352978_19352980delinsCTG	GRCh38
NC_000023.10:g.19371096_19371098delinsCTG , CM000685.1:g.19371096_19371098delinsCTG	GRCh37
NC_000023.9:g.19281017_19281019delinsCTG	NCBI36
NG_016781.1:g.14086_14088delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.440-104_440-102delinsCTG	ENSP00000348062.6:n.440-104_440-102delinsCTG
ENST00000379805.4:c.419-104_419-102delinsCTG	ENSP00000369133.3:n.419-104_419-102delinsCTG
ENST00000417819.6:c.503-104_503-102delinsCTG	ENSP00000404616.2:n.503-104_503-102delinsCTG
ENST00000423505.6:c.533-104_533-102delinsCTG	ENSP00000406473.2:n.533-104_533-102delinsCTG
ENST00000696704.1:c.418+1571_418+1573delinsCTG	ENSP00000512823.1:n.418+1571_418+1573delinsCTG
ENST00000696705.1:c.419-1513_419-1511delinsCTG	ENSP00000512824.1:n.419-1513_419-1511delinsCTG
ENST00000422285.7:c.419-104_419-102delinsCTG MANE Select	ENSP00000394382.2:n.419-104_419-102delinsCTG
ENST00000355808.9:c.440-104_440-102delinsCTG	ENSP00000348062.5:n.440-104_440-102delinsCTG
ENST00000379805.3:c.419-104_419-102delinsCTG	ENSP00000369133.3:n.419-104_419-102delinsCTG
ENST00000379806.9:c.533-104_533-102delinsCTG	ENSP00000369134.5:n.533-104_533-102delinsCTG
ENST00000422285.6:c.419-104_419-102delinsCTG	ENSP00000394382.2:n.419-104_419-102delinsCTG
ENST00000423505.5:c.533-104_533-102delinsCTG	ENSP00000406473.1:n.533-104_533-102delinsCTG
ENST00000479146.1:n.150_152delinsCTG
ENST00000540249.5:c.419-104_419-102delinsCTG	ENSP00000440761.1:n.419-104_419-102delinsCTG
ENST00000545074.5:c.440-104_440-102delinsCTG	ENSP00000438550.1:n.440-104_440-102delinsCTG
NM_000284.3:c.419-104_419-102delinsCTG	NP_000275.1:n.419-104_419-102delinsCTG
NM_001173454.1:c.533-104_533-102delinsCTG	NP_001166925.1:n.533-104_533-102delinsCTG
NM_001173455.1:c.440-104_440-102delinsCTG	NP_001166926.1:n.440-104_440-102delinsCTG
NM_001173456.1:c.419-104_419-102delinsCTG	NP_001166927.1:n.419-104_419-102delinsCTG
XM_011545531.1:c.554-104_554-102delinsCTG	XP_011543833.1:n.554-104_554-102delinsCTG
XM_011545532.1:c.554-104_554-102delinsCTG	XP_011543834.1:n.554-104_554-102delinsCTG
XM_017029574.2:c.533-104_533-102delinsCTG	XP_016885063.1:n.533-104_533-102delinsCTG
NM_000284.4:c.419-104_419-102delinsCTG MANE Select	NP_000275.1:n.419-104_419-102delinsCTG
NM_001173454.2:c.533-104_533-102delinsCTG	NP_001166925.1:n.533-104_533-102delinsCTG
NM_001173455.2:c.440-104_440-102delinsCTG	NP_001166926.1:n.440-104_440-102delinsCTG
NM_001173456.2:c.419-104_419-102delinsCTG	NP_001166927.1:n.419-104_419-102delinsCTG