Canonical Allele Identifier: CA412396219

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377105T>A (hg19) ; chrX:g.19358987T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358987T>A , CM000685.2:g.19358987T>A	GRCh38
NC_000023.10:g.19377105T>A , CM000685.1:g.19377105T>A	GRCh37
NC_000023.9:g.19287026T>A	NCBI36
NG_016781.1:g.20095T>A
NG_021184.1:g.161275A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.992T>A	ENSP00000348062.6:p.Met331Lys
ENST00000379805.4:c.*663T>A	ENSP00000369133.3:n.*663T>A
ENST00000417819.6:c.1055T>A	ENSP00000404616.2:p.Met352Lys
ENST00000423505.6:c.1085T>A	ENSP00000406473.2:p.Met362Lys
ENST00000481733.2:n.766T>A
ENST00000696704.1:c.*303T>A	ENSP00000512823.1:n.*303T>A
ENST00000696705.1:c.*426T>A	ENSP00000512824.1:n.*426T>A
ENST00000422285.7:c.971T>A MANE Select	ENSP00000394382.2:p.Met324Lys
ENST00000379804.1:c.128T>A	ENSP00000369132.1:p.Met43Lys
ENST00000379806.9:c.1085T>A	ENSP00000369134.5:p.Met362Lys
ENST00000422285.6:c.971T>A	ENSP00000394382.2:p.Met324Lys
ENST00000478795.1:n.410T>A
ENST00000481733.1:n.399T>A
ENST00000540249.5:c.878T>A	ENSP00000440761.1:p.Met293Lys
ENST00000545074.5:c.992T>A	ENSP00000438550.1:p.Met331Lys
NM_000284.3:c.971T>A	NP_000275.1:p.Met324Lys
NM_001173454.1:c.1085T>A	NP_001166925.1:p.Met362Lys
NM_001173455.1:c.992T>A	NP_001166926.1:p.Met331Lys
NM_001173456.1:c.878T>A	NP_001166927.1:p.Met293Lys
XM_011545531.1:c.1106T>A	XP_011543833.1:p.Met369Lys
XM_011545532.1:c.1013T>A	XP_011543834.1:p.Met338Lys
XM_017029574.2:c.992T>A	XP_016885063.1:p.Met331Lys
NM_000284.4:c.971T>A MANE Select	NP_000275.1:p.Met324Lys
NM_001173454.2:c.1085T>A	NP_001166925.1:p.Met362Lys
NM_001173455.2:c.992T>A	NP_001166926.1:p.Met331Lys
NM_001173456.2:c.878T>A	NP_001166927.1:p.Met293Lys