Canonical Allele Identifier: CA515485997

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373496A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355378A>T , CM000685.2:g.19355378A>T	GRCh38
NC_000023.10:g.19373496A>T , CM000685.1:g.19373496A>T	GRCh37
NC_000023.9:g.19283417A>T	NCBI36
NG_016781.1:g.16486A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.654A>T	ENSP00000348062.6:p.Ala218=
ENST00000379805.4:c.*325A>T	ENSP00000369133.3:n.*325A>T
ENST00000417819.6:c.717A>T	ENSP00000404616.2:p.Ala239=
ENST00000423505.6:c.747A>T	ENSP00000406473.2:p.Ala249=
ENST00000481733.2:n.428A>T
ENST00000696704.1:c.448A>T	ENSP00000512823.1:p.Ser150Cys
ENST00000696705.1:c.*88A>T	ENSP00000512824.1:n.*88A>T
ENST00000422285.7:c.633A>T MANE Select	ENSP00000394382.2:p.Ala211=
ENST00000379806.9:c.747A>T	ENSP00000369134.5:p.Ala249=
ENST00000422285.6:c.633A>T	ENSP00000394382.2:p.Ala211=
ENST00000479146.1:n.468A>T
ENST00000481733.1:n.61A>T
ENST00000540249.5:c.540A>T	ENSP00000440761.1:p.Ala180=
ENST00000545074.5:c.654A>T	ENSP00000438550.1:p.Ala218=
NM_000284.3:c.633A>T	NP_000275.1:p.Ala211=
NM_001173454.1:c.747A>T	NP_001166925.1:p.Ala249=
NM_001173455.1:c.654A>T	NP_001166926.1:p.Ala218=
NM_001173456.1:c.540A>T	NP_001166927.1:p.Ala180=
XM_011545531.1:c.768A>T	XP_011543833.1:p.Ala256=
XM_011545532.1:c.675A>T	XP_011543834.1:p.Ala225=
XM_017029574.2:c.654A>T	XP_016885063.1:p.Ala218=
NM_000284.4:c.633A>T MANE Select	NP_000275.1:p.Ala211=
NM_001173454.2:c.747A>T	NP_001166925.1:p.Ala249=
NM_001173455.2:c.654A>T	NP_001166926.1:p.Ala218=
NM_001173456.2:c.540A>T	NP_001166927.1:p.Ala180=