Canonical Allele Identifier: CA1963498690

Gene: PDHX

Linked Data

• dbSNP Id: rs1855848128

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34995863A>T , CM000673.2:g.34995863A>T	GRCh38
NC_000011.9:g.35017410A>T , CM000673.1:g.35017410A>T	GRCh37
NC_000011.8:g.34973986A>T	NCBI36
NG_013368.1:g.84734A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.*691A>T	ENSP00000389404.3:n.*691A>T
ENST00000227868.9:c.*691A>T MANE Select	ENSP00000227868.4:n.*691A>T
ENST00000227868.8:c.*691A>T	ENSP00000227868.4:n.*691A>T
ENST00000448838.7:c.*691A>T	ENSP00000389404.2:n.*691A>T
ENST00000477173.3:n.161+3484A>T
NM_001135024.1:c.*691A>T	NP_001128496.1:n.*691A>T
NM_001166158.1:c.*691A>T	NP_001159630.1:n.*691A>T
NM_003477.2:c.*691A>T	NP_003468.2:n.*691A>T
XM_011520390.1:c.*691A>T	XP_011518692.1:n.*691A>T
NM_003477.3:c.*691A>T MANE Select	NP_003468.2:n.*691A>T
NM_001135024.2:c.*691A>T	NP_001128496.2:n.*691A>T
NM_001166158.2:c.*691A>T	NP_001159630.1:n.*691A>T