Canonical Allele Identifier: CA515486435

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377669T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359551T>A , CM000685.2:g.19359551T>A	GRCh38
NC_000023.10:g.19377669T>A , CM000685.1:g.19377669T>A	GRCh37
NC_000023.9:g.19287590T>A	NCBI36
NG_016781.1:g.20659T>A
NG_021184.1:g.160711A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1092T>A	ENSP00000348062.6:p.Pro364=
ENST00000379805.4:c.*763T>A	ENSP00000369133.3:n.*763T>A
ENST00000417819.6:c.1155T>A	ENSP00000404616.2:p.Pro385=
ENST00000423505.6:c.1185T>A	ENSP00000406473.2:p.Pro395=
ENST00000481733.2:n.866T>A
ENST00000696704.1:c.*403T>A	ENSP00000512823.1:n.*403T>A
ENST00000696705.1:c.*526T>A	ENSP00000512824.1:n.*526T>A
ENST00000422285.7:c.1071T>A MANE Select	ENSP00000394382.2:p.Pro357=
ENST00000379804.1:c.228T>A	ENSP00000369132.1:p.Pro76=
ENST00000379806.9:c.1185T>A	ENSP00000369134.5:p.Pro395=
ENST00000422285.6:c.1071T>A	ENSP00000394382.2:p.Pro357=
ENST00000478795.1:n.510T>A
ENST00000540249.5:c.978T>A	ENSP00000440761.1:p.Pro326=
ENST00000545074.5:c.1092T>A	ENSP00000438550.1:p.Pro364=
NM_000284.3:c.1071T>A	NP_000275.1:p.Pro357=
NM_001173454.1:c.1185T>A	NP_001166925.1:p.Pro395=
NM_001173455.1:c.1092T>A	NP_001166926.1:p.Pro364=
NM_001173456.1:c.978T>A	NP_001166927.1:p.Pro326=
XM_011545531.1:c.1206T>A	XP_011543833.1:p.Pro402=
XM_011545532.1:c.1113T>A	XP_011543834.1:p.Pro371=
XM_017029574.2:c.1092T>A	XP_016885063.1:p.Pro364=
NM_000284.4:c.1071T>A MANE Select	NP_000275.1:p.Pro357=
NM_001173454.2:c.1185T>A	NP_001166925.1:p.Pro395=
NM_001173455.2:c.1092T>A	NP_001166926.1:p.Pro364=
NM_001173456.2:c.978T>A	NP_001166927.1:p.Pro326=