Canonical Allele Identifier: CA412396532

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377646G>T (hg19) ; chrX:g.19359528G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359528G>T , CM000685.2:g.19359528G>T	GRCh38
NC_000023.10:g.19377646G>T , CM000685.1:g.19377646G>T	GRCh37
NC_000023.9:g.19287567G>T	NCBI36
NG_016781.1:g.20636G>T
NG_021184.1:g.160734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.1069G>T	ENSP00000348062.6:p.Ala357Ser
ENST00000379805.4:c.*740G>T	ENSP00000369133.3:n.*740G>T
ENST00000417819.6:c.1132G>T	ENSP00000404616.2:p.Ala378Ser
ENST00000423505.6:c.1162G>T	ENSP00000406473.2:p.Ala388Ser
ENST00000481733.2:n.843G>T
ENST00000696704.1:c.*380G>T	ENSP00000512823.1:n.*380G>T
ENST00000696705.1:c.*503G>T	ENSP00000512824.1:n.*503G>T
ENST00000422285.7:c.1048G>T MANE Select	ENSP00000394382.2:p.Ala350Ser
ENST00000379804.1:c.205G>T	ENSP00000369132.1:p.Ala69Ser
ENST00000379806.9:c.1162G>T	ENSP00000369134.5:p.Ala388Ser
ENST00000422285.6:c.1048G>T	ENSP00000394382.2:p.Ala350Ser
ENST00000478795.1:n.487G>T
ENST00000540249.5:c.955G>T	ENSP00000440761.1:p.Ala319Ser
ENST00000545074.5:c.1069G>T	ENSP00000438550.1:p.Ala357Ser
NM_000284.3:c.1048G>T	NP_000275.1:p.Ala350Ser
NM_001173454.1:c.1162G>T	NP_001166925.1:p.Ala388Ser
NM_001173455.1:c.1069G>T	NP_001166926.1:p.Ala357Ser
NM_001173456.1:c.955G>T	NP_001166927.1:p.Ala319Ser
XM_011545531.1:c.1183G>T	XP_011543833.1:p.Ala395Ser
XM_011545532.1:c.1090G>T	XP_011543834.1:p.Ala364Ser
XM_017029574.2:c.1069G>T	XP_016885063.1:p.Ala357Ser
NM_000284.4:c.1048G>T MANE Select	NP_000275.1:p.Ala350Ser
NM_001173454.2:c.1162G>T	NP_001166925.1:p.Ala388Ser
NM_001173455.2:c.1069G>T	NP_001166926.1:p.Ala357Ser
NM_001173456.2:c.955G>T	NP_001166927.1:p.Ala319Ser