Canonical Allele Identifier: CA1963498684
Gene: PDHX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34995852_34995856delinsATTTC , CM000673.2:g.34995852_34995856delinsATTTC GRCh38
NC_000011.9:g.35017399_35017403delinsATTTC , CM000673.1:g.35017399_35017403delinsATTTC GRCh37
NC_000011.8:g.34973975_34973979delinsATTTC NCBI36
NG_013368.1:g.84723_84727delinsATTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.*680_*684delinsATTTC ENSP00000389404.3:n.*680_*684delinsATTTC
ENST00000227868.9:c.*680_*684delinsATTTC MANE Select ENSP00000227868.4:n.*680_*684delinsATTTC
ENST00000227868.8:c.*680_*684delinsATTTC ENSP00000227868.4:n.*680_*684delinsATTTC
ENST00000448838.7:c.*680_*684delinsATTTC ENSP00000389404.2:n.*680_*684delinsATTTC
ENST00000477173.3:n.161+3473_161+3477delinsATTTC
NM_001135024.1:c.*680_*684delinsATTTC NP_001128496.1:n.*680_*684delinsATTTC
NM_001166158.1:c.*680_*684delinsATTTC NP_001159630.1:n.*680_*684delinsATTTC
NM_003477.2:c.*680_*684delinsATTTC NP_003468.2:n.*680_*684delinsATTTC
XM_011520390.1:c.*680_*684delinsATTTC XP_011518692.1:n.*680_*684delinsATTTC
NM_003477.3:c.*680_*684delinsATTTC MANE Select NP_003468.2:n.*680_*684delinsATTTC
NM_001135024.2:c.*680_*684delinsATTTC NP_001128496.2:n.*680_*684delinsATTTC
NM_001166158.2:c.*680_*684delinsATTTC NP_001159630.1:n.*680_*684delinsATTTC