Canonical Allele Identifier: CA412396374

Gene: PDHA1

Linked Data

• gnomAD v4: X-19359495-G-A
• MyVariant Identifiers: chrX:g.19377613G>A (hg19) ; chrX:g.19359495G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359495G>A , CM000685.2:g.19359495G>A	GRCh38
NC_000023.10:g.19377613G>A , CM000685.1:g.19377613G>A	GRCh37
NC_000023.9:g.19287534G>A	NCBI36
NG_016781.1:g.20603G>A
NG_021184.1:g.160767C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.1036G>A	ENSP00000348062.6:p.Asp346Asn
ENST00000379805.4:c.*707G>A	ENSP00000369133.3:n.*707G>A
ENST00000417819.6:c.1099G>A	ENSP00000404616.2:p.Asp367Asn
ENST00000423505.6:c.1129G>A	ENSP00000406473.2:p.Asp377Asn
ENST00000481733.2:n.810G>A
ENST00000696704.1:c.*347G>A	ENSP00000512823.1:n.*347G>A
ENST00000696705.1:c.*470G>A	ENSP00000512824.1:n.*470G>A
ENST00000422285.7:c.1015G>A MANE Select	ENSP00000394382.2:p.Asp339Asn
ENST00000379804.1:c.172G>A	ENSP00000369132.1:p.Asp58Asn
ENST00000379806.9:c.1129G>A	ENSP00000369134.5:p.Asp377Asn
ENST00000422285.6:c.1015G>A	ENSP00000394382.2:p.Asp339Asn
ENST00000478795.1:n.454G>A
ENST00000540249.5:c.922G>A	ENSP00000440761.1:p.Asp308Asn
ENST00000545074.5:c.1036G>A	ENSP00000438550.1:p.Asp346Asn
NM_000284.3:c.1015G>A	NP_000275.1:p.Asp339Asn
NM_001173454.1:c.1129G>A	NP_001166925.1:p.Asp377Asn
NM_001173455.1:c.1036G>A	NP_001166926.1:p.Asp346Asn
NM_001173456.1:c.922G>A	NP_001166927.1:p.Asp308Asn
XM_011545531.1:c.1150G>A	XP_011543833.1:p.Asp384Asn
XM_011545532.1:c.1057G>A	XP_011543834.1:p.Asp353Asn
XM_017029574.2:c.1036G>A	XP_016885063.1:p.Asp346Asn
NM_000284.4:c.1015G>A MANE Select	NP_000275.1:p.Asp339Asn
NM_001173454.2:c.1129G>A	NP_001166925.1:p.Asp377Asn
NM_001173455.2:c.1036G>A	NP_001166926.1:p.Asp346Asn
NM_001173456.2:c.922G>A	NP_001166927.1:p.Asp308Asn