Canonical Allele Identifier: CA412396134

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377069G>C (hg19) ; chrX:g.19358951G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358951G>C , CM000685.2:g.19358951G>C	GRCh38
NC_000023.10:g.19377069G>C , CM000685.1:g.19377069G>C	GRCh37
NC_000023.9:g.19286990G>C	NCBI36
NG_016781.1:g.20059G>C
NG_021184.1:g.161311C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.956G>C	ENSP00000348062.6:p.Ser319Thr
ENST00000379805.4:c.*627G>C	ENSP00000369133.3:n.*627G>C
ENST00000417819.6:c.1019G>C	ENSP00000404616.2:p.Ser340Thr
ENST00000423505.6:c.1049G>C	ENSP00000406473.2:p.Ser350Thr
ENST00000481733.2:n.730G>C
ENST00000696704.1:c.*267G>C	ENSP00000512823.1:n.*267G>C
ENST00000696705.1:c.*390G>C	ENSP00000512824.1:n.*390G>C
ENST00000422285.7:c.935G>C MANE Select	ENSP00000394382.2:p.Ser312Thr
ENST00000379804.1:c.92G>C	ENSP00000369132.1:p.Ser31Thr
ENST00000379806.9:c.1049G>C	ENSP00000369134.5:p.Ser350Thr
ENST00000422285.6:c.935G>C	ENSP00000394382.2:p.Ser312Thr
ENST00000478795.1:n.374G>C
ENST00000481733.1:n.363G>C
ENST00000540249.5:c.842G>C	ENSP00000440761.1:p.Ser281Thr
ENST00000545074.5:c.956G>C	ENSP00000438550.1:p.Ser319Thr
NM_000284.3:c.935G>C	NP_000275.1:p.Ser312Thr
NM_001173454.1:c.1049G>C	NP_001166925.1:p.Ser350Thr
NM_001173455.1:c.956G>C	NP_001166926.1:p.Ser319Thr
NM_001173456.1:c.842G>C	NP_001166927.1:p.Ser281Thr
XM_011545531.1:c.1070G>C	XP_011543833.1:p.Ser357Thr
XM_011545532.1:c.977G>C	XP_011543834.1:p.Ser326Thr
XM_017029574.2:c.956G>C	XP_016885063.1:p.Ser319Thr
NM_000284.4:c.935G>C MANE Select	NP_000275.1:p.Ser312Thr
NM_001173454.2:c.1049G>C	NP_001166925.1:p.Ser350Thr
NM_001173455.2:c.956G>C	NP_001166926.1:p.Ser319Thr
NM_001173456.2:c.842G>C	NP_001166927.1:p.Ser281Thr