Canonical Allele Identifier: CA412396272

Gene: PDHA1

Linked Data

• gnomAD v4: X-19359010-G-A
• MyVariant Identifiers: chrX:g.19377128G>A (hg19) ; chrX:g.19359010G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359010G>A , CM000685.2:g.19359010G>A	GRCh38
NC_000023.10:g.19377128G>A , CM000685.1:g.19377128G>A	GRCh37
NC_000023.9:g.19287049G>A	NCBI36
NG_016781.1:g.20118G>A
NG_021184.1:g.161252C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1015G>A	ENSP00000348062.6:p.Val339Met
ENST00000379805.4:c.*686G>A	ENSP00000369133.3:n.*686G>A
ENST00000417819.6:c.1078G>A	ENSP00000404616.2:p.Val360Met
ENST00000423505.6:c.1108G>A	ENSP00000406473.2:p.Val370Met
ENST00000481733.2:n.789G>A
ENST00000696704.1:c.*326G>A	ENSP00000512823.1:n.*326G>A
ENST00000696705.1:c.*449G>A	ENSP00000512824.1:n.*449G>A
ENST00000422285.7:c.994G>A MANE Select	ENSP00000394382.2:p.Val332Met
ENST00000379804.1:c.151G>A	ENSP00000369132.1:p.Val51Met
ENST00000379806.9:c.1108G>A	ENSP00000369134.5:p.Val370Met
ENST00000422285.6:c.994G>A	ENSP00000394382.2:p.Val332Met
ENST00000478795.1:n.433G>A
ENST00000481733.1:n.422G>A
ENST00000540249.5:c.901G>A	ENSP00000440761.1:p.Val301Met
ENST00000545074.5:c.1015G>A	ENSP00000438550.1:p.Val339Met
NM_000284.3:c.994G>A	NP_000275.1:p.Val332Met
NM_001173454.1:c.1108G>A	NP_001166925.1:p.Val370Met
NM_001173455.1:c.1015G>A	NP_001166926.1:p.Val339Met
NM_001173456.1:c.901G>A	NP_001166927.1:p.Val301Met
XM_011545531.1:c.1129G>A	XP_011543833.1:p.Val377Met
XM_011545532.1:c.1036G>A	XP_011543834.1:p.Val346Met
XM_017029574.2:c.1015G>A	XP_016885063.1:p.Val339Met
NM_000284.4:c.994G>A MANE Select	NP_000275.1:p.Val332Met
NM_001173454.2:c.1108G>A	NP_001166925.1:p.Val370Met
NM_001173455.2:c.1015G>A	NP_001166926.1:p.Val339Met
NM_001173456.2:c.901G>A	NP_001166927.1:p.Val301Met