Canonical Allele Identifier: CA2693251447

Gene: PDHA1

Linked Data

• gnomAD v4: X-19359808-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359808T>A , CM000685.2:g.19359808T>A	GRCh38
NC_000023.10:g.19377926T>A , CM000685.1:g.19377926T>A	GRCh37
NC_000023.9:g.19287847T>A	NCBI36
NG_016781.1:g.20916T>A
NG_021184.1:g.160454A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*155T>A	ENSP00000348062.6:n.*155T>A
ENST00000417819.6:c.*155T>A	ENSP00000404616.2:n.*155T>A
ENST00000423505.6:c.*155T>A	ENSP00000406473.2:n.*155T>A
ENST00000481733.2:n.1123T>A
ENST00000696704.1:c.*660T>A	ENSP00000512823.1:n.*660T>A
ENST00000696705.1:c.*783T>A	ENSP00000512824.1:n.*783T>A
ENST00000422285.7:c.*155T>A MANE Select	ENSP00000394382.2:n.*155T>A
ENST00000379804.1:c.*155T>A	ENSP00000369132.1:n.*155T>A
ENST00000379806.9:c.*155T>A	ENSP00000369134.5:n.*155T>A
ENST00000422285.6:c.*155T>A	ENSP00000394382.2:n.*155T>A
ENST00000478795.1:n.767T>A
ENST00000540249.5:c.*155T>A	ENSP00000440761.1:n.*155T>A
ENST00000545074.5:c.*155T>A	ENSP00000438550.1:n.*155T>A
NM_000284.3:c.*155T>A	NP_000275.1:n.*155T>A
NM_001173454.1:c.*155T>A	NP_001166925.1:n.*155T>A
NM_001173455.1:c.*155T>A	NP_001166926.1:n.*155T>A
NM_001173456.1:c.*155T>A	NP_001166927.1:n.*155T>A
XM_011545531.1:c.*155T>A	XP_011543833.1:n.*155T>A
XM_011545532.1:c.*155T>A	XP_011543834.1:n.*155T>A
XM_017029574.2:c.*155T>A	XP_016885063.1:n.*155T>A
NM_000284.4:c.*155T>A MANE Select	NP_000275.1:n.*155T>A
NM_001173454.2:c.*155T>A	NP_001166925.1:n.*155T>A
NM_001173455.2:c.*155T>A	NP_001166926.1:n.*155T>A
NM_001173456.2:c.*155T>A	NP_001166927.1:n.*155T>A