Canonical Allele Identifier: CA380123976

Gene: PDHX

Linked Data

• MyVariant Identifiers: chr11:g.34938328T>G (hg19) ; chr11:g.34916781T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916781T>G , CM000673.2:g.34916781T>G	GRCh38
NC_000011.9:g.34938328T>G , CM000673.1:g.34938328T>G	GRCh37
NC_000011.8:g.34894904T>G	NCBI36
NG_013368.1:g.5652T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.-21+295T>G	ENSP00000389404.3:n.-21+295T>G
ENST00000227868.9:c.126T>G MANE Select	ENSP00000227868.4:p.Asn42Lys
ENST00000227868.8:c.126T>G	ENSP00000227868.4:p.Asn42Lys
ENST00000430469.6:c.126T>G	ENSP00000415695.2:p.Asn42Lys
ENST00000448838.7:c.115+295T>G	ENSP00000389404.2:n.115+295T>G
ENST00000533262.1:c.126T>G	ENSP00000432277.1:p.Asn42Lys
ENST00000533550.5:c.-21+843T>G	ENSP00000431281.1:n.-21+843T>G
NM_001135024.1:c.115+295T>G	NP_001128496.1:n.115+295T>G
NM_001166158.1:c.126T>G	NP_001159630.1:p.Asn42Lys
NM_003477.2:c.126T>G	NP_003468.2:p.Asn42Lys
XM_011520390.1:c.-21+843T>G	XP_011518692.1:n.-21+843T>G
NM_003477.3:c.126T>G MANE Select	NP_003468.2:p.Asn42Lys
NM_001135024.2:c.-21+295T>G	NP_001128496.2:n.-21+295T>G
NM_001166158.2:c.126T>G	NP_001159630.1:p.Asn42Lys