Canonical Allele Identifier: CA5945933

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34960495C>G , CM000673.2:g.34960495C>G	GRCh38
NC_000011.9:g.34982042C>G , CM000673.1:g.34982042C>G	GRCh37
NC_000011.8:g.34938618C>G	NCBI36
NG_013368.1:g.49366C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.438C>G	ENSP00000389404.3:p.Gly146=
ENST00000227868.9:c.618C>G MANE Select	ENSP00000227868.4:p.Gly206=
ENST00000227868.8:c.618C>G	ENSP00000227868.4:p.Gly206=
ENST00000430469.6:c.342+12889C>G	ENSP00000415695.2:n.342+12889C>G
ENST00000448838.7:c.573C>G	ENSP00000389404.2:p.Gly191=
ENST00000533262.1:c.537C>G	ENSP00000432277.1:p.Gly179=
ENST00000533550.5:c.438C>G	ENSP00000431281.1:p.Gly146=
NM_001135024.1:c.573C>G	NP_001128496.1:p.Gly191=
NM_001166158.1:c.342+12889C>G	NP_001159630.1:n.342+12889C>G
NM_003477.2:c.618C>G	NP_003468.2:p.Gly206=
XM_011520390.1:c.438C>G	XP_011518692.1:p.Gly146=
NM_003477.3:c.618C>G MANE Select	NP_003468.2:p.Gly206=
NM_001135024.2:c.438C>G	NP_001128496.2:p.Gly146=
NM_001166158.2:c.342+12889C>G	NP_001159630.1:n.342+12889C>G