Canonical Allele Identifier: CA412394580

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373568A>T (hg19) ; chrX:g.19355450A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355450A>T , CM000685.2:g.19355450A>T	GRCh38
NC_000023.10:g.19373568A>T , CM000685.1:g.19373568A>T	GRCh37
NC_000023.9:g.19283489A>T	NCBI36
NG_016781.1:g.16558A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.726A>T	ENSP00000348062.6:p.Arg242Ser
ENST00000379805.4:c.*397A>T	ENSP00000369133.3:n.*397A>T
ENST00000417819.6:c.789A>T	ENSP00000404616.2:p.Arg263Ser
ENST00000423505.6:c.819A>T	ENSP00000406473.2:p.Arg273Ser
ENST00000481733.2:n.500A>T
ENST00000696704.1:c.*37A>T	ENSP00000512823.1:n.*37A>T
ENST00000696705.1:c.*160A>T	ENSP00000512824.1:n.*160A>T
ENST00000422285.7:c.705A>T MANE Select	ENSP00000394382.2:p.Arg235Ser
ENST00000379806.9:c.819A>T	ENSP00000369134.5:p.Arg273Ser
ENST00000422285.6:c.705A>T	ENSP00000394382.2:p.Arg235Ser
ENST00000481733.1:n.133A>T
ENST00000540249.5:c.612A>T	ENSP00000440761.1:p.Arg204Ser
ENST00000545074.5:c.726A>T	ENSP00000438550.1:p.Arg242Ser
NM_000284.3:c.705A>T	NP_000275.1:p.Arg235Ser
NM_001173454.1:c.819A>T	NP_001166925.1:p.Arg273Ser
NM_001173455.1:c.726A>T	NP_001166926.1:p.Arg242Ser
NM_001173456.1:c.612A>T	NP_001166927.1:p.Arg204Ser
XM_011545531.1:c.840A>T	XP_011543833.1:p.Arg280Ser
XM_011545532.1:c.747A>T	XP_011543834.1:p.Arg249Ser
XM_017029574.2:c.726A>T	XP_016885063.1:p.Arg242Ser
NM_000284.4:c.705A>T MANE Select	NP_000275.1:p.Arg235Ser
NM_001173454.2:c.819A>T	NP_001166925.1:p.Arg273Ser
NM_001173455.2:c.726A>T	NP_001166926.1:p.Arg242Ser
NM_001173456.2:c.612A>T	NP_001166927.1:p.Arg204Ser