Canonical Allele Identifier: CA1963422153

Gene: PDHX APIP

Linked Data

• dbSNP Id: rs1853703792
• gnomAD v4: 11-34916485-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916485A>G , CM000673.2:g.34916485A>G	GRCh38
NC_000011.9:g.34938032A>G , CM000673.1:g.34938032A>G	GRCh37
NC_000011.8:g.34894608A>G	NCBI36
NG_013368.1:g.5356A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.-22A>G (PDHX)	ENSP00000389404.3:n.-22A>G
ENST00000395787.3:c.-201T>C (APIP)	ENSP00000379133.3:n.-201T>C
ENST00000448838.7:c.114A>G (PDHX)	ENSP00000389404.2:p.Gly38=
ENST00000533550.5:c.-21+547A>G (PDHX)	ENSP00000431281.1:n.-21+547A>G
NM_001135024.1:c.114A>G (PDHX)	NP_001128496.1:p.Gly38=
NM_001166158.1:c.-171A>G (PDHX)	NP_001159630.1:n.-171A>G
NM_003477.2:c.-171A>G (PDHX)	NP_003468.2:n.-171A>G
XM_011520390.1:c.-21+547A>G (PDHX)	XP_011518692.1:n.-21+547A>G
NM_001135024.2:c.-22A>G (PDHX)	NP_001128496.2:n.-22A>G