Canonical Allele Identifier: CA412396535

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377647C>A (hg19) ; chrX:g.19359529C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359529C>A , CM000685.2:g.19359529C>A	GRCh38
NC_000023.10:g.19377647C>A , CM000685.1:g.19377647C>A	GRCh37
NC_000023.9:g.19287568C>A	NCBI36
NG_016781.1:g.20637C>A
NG_021184.1:g.160733G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1070C>A	ENSP00000348062.6:p.Ala357Asp
ENST00000379805.4:c.*741C>A	ENSP00000369133.3:n.*741C>A
ENST00000417819.6:c.1133C>A	ENSP00000404616.2:p.Ala378Asp
ENST00000423505.6:c.1163C>A	ENSP00000406473.2:p.Ala388Asp
ENST00000481733.2:n.844C>A
ENST00000696704.1:c.*381C>A	ENSP00000512823.1:n.*381C>A
ENST00000696705.1:c.*504C>A	ENSP00000512824.1:n.*504C>A
ENST00000422285.7:c.1049C>A MANE Select	ENSP00000394382.2:p.Ala350Asp
ENST00000379804.1:c.206C>A	ENSP00000369132.1:p.Ala69Asp
ENST00000379806.9:c.1163C>A	ENSP00000369134.5:p.Ala388Asp
ENST00000422285.6:c.1049C>A	ENSP00000394382.2:p.Ala350Asp
ENST00000478795.1:n.488C>A
ENST00000540249.5:c.956C>A	ENSP00000440761.1:p.Ala319Asp
ENST00000545074.5:c.1070C>A	ENSP00000438550.1:p.Ala357Asp
NM_000284.3:c.1049C>A	NP_000275.1:p.Ala350Asp
NM_001173454.1:c.1163C>A	NP_001166925.1:p.Ala388Asp
NM_001173455.1:c.1070C>A	NP_001166926.1:p.Ala357Asp
NM_001173456.1:c.956C>A	NP_001166927.1:p.Ala319Asp
XM_011545531.1:c.1184C>A	XP_011543833.1:p.Ala395Asp
XM_011545532.1:c.1091C>A	XP_011543834.1:p.Ala364Asp
XM_017029574.2:c.1070C>A	XP_016885063.1:p.Ala357Asp
NM_000284.4:c.1049C>A MANE Select	NP_000275.1:p.Ala350Asp
NM_001173454.2:c.1163C>A	NP_001166925.1:p.Ala388Asp
NM_001173455.2:c.1070C>A	NP_001166926.1:p.Ala357Asp
NM_001173456.2:c.956C>A	NP_001166927.1:p.Ala319Asp