Canonical Allele Identifier: CA412396575

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377655G>C (hg19) ; chrX:g.19359537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359537G>C , CM000685.2:g.19359537G>C	GRCh38
NC_000023.10:g.19377655G>C , CM000685.1:g.19377655G>C	GRCh37
NC_000023.9:g.19287576G>C	NCBI36
NG_016781.1:g.20645G>C
NG_021184.1:g.160725C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.1078G>C	ENSP00000348062.6:p.Ala360Pro
ENST00000379805.4:c.*749G>C	ENSP00000369133.3:n.*749G>C
ENST00000417819.6:c.1141G>C	ENSP00000404616.2:p.Ala381Pro
ENST00000423505.6:c.1171G>C	ENSP00000406473.2:p.Ala391Pro
ENST00000481733.2:n.852G>C
ENST00000696704.1:c.*389G>C	ENSP00000512823.1:n.*389G>C
ENST00000696705.1:c.*512G>C	ENSP00000512824.1:n.*512G>C
ENST00000422285.7:c.1057G>C MANE Select	ENSP00000394382.2:p.Ala353Pro
ENST00000379804.1:c.214G>C	ENSP00000369132.1:p.Ala72Pro
ENST00000379806.9:c.1171G>C	ENSP00000369134.5:p.Ala391Pro
ENST00000422285.6:c.1057G>C	ENSP00000394382.2:p.Ala353Pro
ENST00000478795.1:n.496G>C
ENST00000540249.5:c.964G>C	ENSP00000440761.1:p.Ala322Pro
ENST00000545074.5:c.1078G>C	ENSP00000438550.1:p.Ala360Pro
NM_000284.3:c.1057G>C	NP_000275.1:p.Ala353Pro
NM_001173454.1:c.1171G>C	NP_001166925.1:p.Ala391Pro
NM_001173455.1:c.1078G>C	NP_001166926.1:p.Ala360Pro
NM_001173456.1:c.964G>C	NP_001166927.1:p.Ala322Pro
XM_011545531.1:c.1192G>C	XP_011543833.1:p.Ala398Pro
XM_011545532.1:c.1099G>C	XP_011543834.1:p.Ala367Pro
XM_017029574.2:c.1078G>C	XP_016885063.1:p.Ala360Pro
NM_000284.4:c.1057G>C MANE Select	NP_000275.1:p.Ala353Pro
NM_001173454.2:c.1171G>C	NP_001166925.1:p.Ala391Pro
NM_001173455.2:c.1078G>C	NP_001166926.1:p.Ala360Pro
NM_001173456.2:c.964G>C	NP_001166927.1:p.Ala322Pro