Canonical Allele Identifier: CA412397236

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377745T>C (hg19) ; chrX:g.19359627T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359627T>C , CM000685.2:g.19359627T>C	GRCh38
NC_000023.10:g.19377745T>C , CM000685.1:g.19377745T>C	GRCh37
NC_000023.9:g.19287666T>C	NCBI36
NG_016781.1:g.20735T>C
NG_021184.1:g.160635A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1168T>C	ENSP00000348062.6:p.Trp390Arg
ENST00000379805.4:c.*839T>C	ENSP00000369133.3:n.*839T>C
ENST00000417819.6:c.1231T>C	ENSP00000404616.2:p.Trp411Arg
ENST00000423505.6:c.1261T>C	ENSP00000406473.2:p.Trp421Arg
ENST00000481733.2:n.942T>C
ENST00000696704.1:c.*479T>C	ENSP00000512823.1:n.*479T>C
ENST00000696705.1:c.*602T>C	ENSP00000512824.1:n.*602T>C
ENST00000422285.7:c.1147T>C MANE Select	ENSP00000394382.2:p.Trp383Arg
ENST00000379804.1:c.304T>C	ENSP00000369132.1:p.Trp102Arg
ENST00000379806.9:c.1261T>C	ENSP00000369134.5:p.Trp421Arg
ENST00000422285.6:c.1147T>C	ENSP00000394382.2:p.Trp383Arg
ENST00000478795.1:n.586T>C
ENST00000540249.5:c.1054T>C	ENSP00000440761.1:p.Trp352Arg
ENST00000545074.5:c.1168T>C	ENSP00000438550.1:p.Trp390Arg
NM_000284.3:c.1147T>C	NP_000275.1:p.Trp383Arg
NM_001173454.1:c.1261T>C	NP_001166925.1:p.Trp421Arg
NM_001173455.1:c.1168T>C	NP_001166926.1:p.Trp390Arg
NM_001173456.1:c.1054T>C	NP_001166927.1:p.Trp352Arg
XM_011545531.1:c.1282T>C	XP_011543833.1:p.Trp428Arg
XM_011545532.1:c.1189T>C	XP_011543834.1:p.Trp397Arg
XM_017029574.2:c.1168T>C	XP_016885063.1:p.Trp390Arg
NM_000284.4:c.1147T>C MANE Select	NP_000275.1:p.Trp383Arg
NM_001173454.2:c.1261T>C	NP_001166925.1:p.Trp421Arg
NM_001173455.2:c.1168T>C	NP_001166926.1:p.Trp390Arg
NM_001173456.2:c.1054T>C	NP_001166927.1:p.Trp352Arg