Canonical Allele Identifier: CA2613091491

Gene: PDHX APIP

Linked Data

• gnomAD v4: 11-34916492-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916492G>T , CM000673.2:g.34916492G>T	GRCh38
NC_000011.9:g.34938039G>T , CM000673.1:g.34938039G>T	GRCh37
NC_000011.8:g.34894615G>T	NCBI36
NG_013368.1:g.5363G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.-21+6G>T (PDHX)	ENSP00000389404.3:n.-21+6G>T
ENST00000395787.3:c.-208C>A (APIP)	ENSP00000379133.3:n.-208C>A
ENST00000448838.7:c.115+6G>T (PDHX)	ENSP00000389404.2:n.115+6G>T
ENST00000533550.5:c.-21+554G>T (PDHX)	ENSP00000431281.1:n.-21+554G>T
NM_001135024.1:c.115+6G>T (PDHX)	NP_001128496.1:n.115+6G>T
NM_001166158.1:c.-164G>T (PDHX)	NP_001159630.1:n.-164G>T
NM_003477.2:c.-164G>T (PDHX)	NP_003468.2:n.-164G>T
XM_011520390.1:c.-21+554G>T (PDHX)	XP_011518692.1:n.-21+554G>T
NM_001135024.2:c.-21+6G>T (PDHX)	NP_001128496.2:n.-21+6G>T