Canonical Allele Identifier: CA515486483

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377741T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359623T>C , CM000685.2:g.19359623T>C	GRCh38
NC_000023.10:g.19377741T>C , CM000685.1:g.19377741T>C	GRCh37
NC_000023.9:g.19287662T>C	NCBI36
NG_016781.1:g.20731T>C
NG_021184.1:g.160639A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1164T>C	ENSP00000348062.6:p.Asn388=
ENST00000379805.4:c.*835T>C	ENSP00000369133.3:n.*835T>C
ENST00000417819.6:c.1227T>C	ENSP00000404616.2:p.Asn409=
ENST00000423505.6:c.1257T>C	ENSP00000406473.2:p.Asn419=
ENST00000481733.2:n.938T>C
ENST00000696704.1:c.*475T>C	ENSP00000512823.1:n.*475T>C
ENST00000696705.1:c.*598T>C	ENSP00000512824.1:n.*598T>C
ENST00000422285.7:c.1143T>C MANE Select	ENSP00000394382.2:p.Asn381=
ENST00000379804.1:c.300T>C	ENSP00000369132.1:p.Asn100=
ENST00000379806.9:c.1257T>C	ENSP00000369134.5:p.Asn419=
ENST00000422285.6:c.1143T>C	ENSP00000394382.2:p.Asn381=
ENST00000478795.1:n.582T>C
ENST00000540249.5:c.1050T>C	ENSP00000440761.1:p.Asn350=
ENST00000545074.5:c.1164T>C	ENSP00000438550.1:p.Asn388=
NM_000284.3:c.1143T>C	NP_000275.1:p.Asn381=
NM_001173454.1:c.1257T>C	NP_001166925.1:p.Asn419=
NM_001173455.1:c.1164T>C	NP_001166926.1:p.Asn388=
NM_001173456.1:c.1050T>C	NP_001166927.1:p.Asn350=
XM_011545531.1:c.1278T>C	XP_011543833.1:p.Asn426=
XM_011545532.1:c.1185T>C	XP_011543834.1:p.Asn395=
XM_017029574.2:c.1164T>C	XP_016885063.1:p.Asn388=
NM_000284.4:c.1143T>C MANE Select	NP_000275.1:p.Asn381=
NM_001173454.2:c.1257T>C	NP_001166925.1:p.Asn419=
NM_001173455.2:c.1164T>C	NP_001166926.1:p.Asn388=
NM_001173456.2:c.1050T>C	NP_001166927.1:p.Asn350=