Canonical Allele Identifier: CA412391069

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19369456G>T (hg19) ; chrX:g.19351338G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19351338G>T , CM000685.2:g.19351338G>T	GRCh38
NC_000023.10:g.19369456G>T , CM000685.1:g.19369456G>T	GRCh37
NC_000023.9:g.19279377G>T	NCBI36
NG_016781.1:g.12446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.370G>T	ENSP00000348062.6:p.Ala124Ser
ENST00000379805.4:c.349G>T	ENSP00000369133.3:p.Ala117Ser
ENST00000417819.6:c.433G>T	ENSP00000404616.2:p.Ala145Ser
ENST00000423505.6:c.463G>T	ENSP00000406473.2:p.Ala155Ser
ENST00000696704.1:c.349G>T	ENSP00000512823.1:p.Ala117Ser
ENST00000696705.1:c.349G>T	ENSP00000512824.1:p.Ala117Ser
ENST00000422285.7:c.349G>T MANE Select	ENSP00000394382.2:p.Ala117Ser
ENST00000355808.9:c.370G>T	ENSP00000348062.5:p.Ala124Ser
ENST00000379805.3:c.349G>T	ENSP00000369133.3:p.Ala117Ser
ENST00000379806.9:c.463G>T	ENSP00000369134.5:p.Ala155Ser
ENST00000422285.6:c.349G>T	ENSP00000394382.2:p.Ala117Ser
ENST00000423505.5:c.463G>T	ENSP00000406473.1:p.Ala155Ser
ENST00000492364.1:n.451G>T
ENST00000540249.5:c.349G>T	ENSP00000440761.1:p.Ala117Ser
ENST00000545074.5:c.370G>T	ENSP00000438550.1:p.Ala124Ser
NM_000284.3:c.349G>T	NP_000275.1:p.Ala117Ser
NM_001173454.1:c.463G>T	NP_001166925.1:p.Ala155Ser
NM_001173455.1:c.370G>T	NP_001166926.1:p.Ala124Ser
NM_001173456.1:c.349G>T	NP_001166927.1:p.Ala117Ser
XM_011545531.1:c.484G>T	XP_011543833.1:p.Ala162Ser
XM_011545532.1:c.484G>T	XP_011543834.1:p.Ala162Ser
XM_017029574.2:c.463G>T	XP_016885063.1:p.Ala155Ser
NM_000284.4:c.349G>T MANE Select	NP_000275.1:p.Ala117Ser
NM_001173454.2:c.463G>T	NP_001166925.1:p.Ala155Ser
NM_001173455.2:c.370G>T	NP_001166926.1:p.Ala124Ser
NM_001173456.2:c.349G>T	NP_001166927.1:p.Ala117Ser