Canonical Allele Identifier: CA515486429

Gene: PDHA1

Linked Data

• COSMIC: COSM1287053 ; COSM1287054
• MyVariant Identifiers: chrX:g.19377657C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359539C>A , CM000685.2:g.19359539C>A	GRCh38
NC_000023.10:g.19377657C>A , CM000685.1:g.19377657C>A	GRCh37
NC_000023.9:g.19287578C>A	NCBI36
NG_016781.1:g.20647C>A
NG_021184.1:g.160723G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.1080C>A	ENSP00000348062.6:p.Ala360=
ENST00000379805.4:c.*751C>A	ENSP00000369133.3:n.*751C>A
ENST00000417819.6:c.1143C>A	ENSP00000404616.2:p.Ala381=
ENST00000423505.6:c.1173C>A	ENSP00000406473.2:p.Ala391=
ENST00000481733.2:n.854C>A
ENST00000696704.1:c.*391C>A	ENSP00000512823.1:n.*391C>A
ENST00000696705.1:c.*514C>A	ENSP00000512824.1:n.*514C>A
ENST00000422285.7:c.1059C>A MANE Select	ENSP00000394382.2:p.Ala353=
ENST00000379804.1:c.216C>A	ENSP00000369132.1:p.Ala72=
ENST00000379806.9:c.1173C>A	ENSP00000369134.5:p.Ala391=
ENST00000422285.6:c.1059C>A	ENSP00000394382.2:p.Ala353=
ENST00000478795.1:n.498C>A
ENST00000540249.5:c.966C>A	ENSP00000440761.1:p.Ala322=
ENST00000545074.5:c.1080C>A	ENSP00000438550.1:p.Ala360=
NM_000284.3:c.1059C>A	NP_000275.1:p.Ala353=
NM_001173454.1:c.1173C>A	NP_001166925.1:p.Ala391=
NM_001173455.1:c.1080C>A	NP_001166926.1:p.Ala360=
NM_001173456.1:c.966C>A	NP_001166927.1:p.Ala322=
XM_011545531.1:c.1194C>A	XP_011543833.1:p.Ala398=
XM_011545532.1:c.1101C>A	XP_011543834.1:p.Ala367=
XM_017029574.2:c.1080C>A	XP_016885063.1:p.Ala360=
NM_000284.4:c.1059C>A MANE Select	NP_000275.1:p.Ala353=
NM_001173454.2:c.1173C>A	NP_001166925.1:p.Ala391=
NM_001173455.2:c.1080C>A	NP_001166926.1:p.Ala360=
NM_001173456.2:c.966C>A	NP_001166927.1:p.Ala322=