Canonical Allele Identifier: CA1963422655

Gene: PDHX

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916741_34916745delinsTGAAG , CM000673.2:g.34916741_34916745delinsTGAAG	GRCh38
NC_000011.9:g.34938288_34938292delinsTGAAG , CM000673.1:g.34938288_34938292delinsTGAAG	GRCh37
NC_000011.8:g.34894864_34894868delinsTGAAG	NCBI36
NG_013368.1:g.5612_5616delinsTGAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000448838.8:c.-21+255_-21+259delinsTGAAG	ENSP00000389404.3:n.-21+255_-21+259delinsTGAAG
ENST00000227868.9:c.86_90delinsTGAAG MANE Select	ENSP00000227868.4:p.Val29=
ENST00000227868.8:c.86_90delinsTGAAG	ENSP00000227868.4:p.Val29=
ENST00000430469.6:c.86_90delinsTGAAG	ENSP00000415695.2:p.Val29=
ENST00000448838.7:c.115+255_115+259delinsTGAAG	ENSP00000389404.2:n.115+255_115+259delinsTGAAG
ENST00000533262.1:c.86_90delinsTGAAG	ENSP00000432277.1:p.Val29=
ENST00000533550.5:c.-21+803_-21+807delinsTGAAG	ENSP00000431281.1:n.-21+803_-21+807delinsTGAAG
NM_001135024.1:c.115+255_115+259delinsTGAAG	NP_001128496.1:n.115+255_115+259delinsTGAAG
NM_001166158.1:c.86_90delinsTGAAG	NP_001159630.1:p.Val29=
NM_003477.2:c.86_90delinsTGAAG	NP_003468.2:p.Val29=
XM_011520390.1:c.-21+803_-21+807delinsTGAAG	XP_011518692.1:n.-21+803_-21+807delinsTGAAG
NM_003477.3:c.86_90delinsTGAAG MANE Select	NP_003468.2:p.Val29=
NM_001135024.2:c.-21+255_-21+259delinsTGAAG	NP_001128496.2:n.-21+255_-21+259delinsTGAAG
NM_001166158.2:c.86_90delinsTGAAG	NP_001159630.1:p.Val29=