Canonical Allele Identifier: CA380123999

Gene: PDHX

Linked Data

• gnomAD v4: 11-34916790-G-T
• MyVariant Identifiers: chr11:g.34938337G>T (hg19) ; chr11:g.34916790G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34916790G>T , CM000673.2:g.34916790G>T	GRCh38
NC_000011.9:g.34938337G>T , CM000673.1:g.34938337G>T	GRCh37
NC_000011.8:g.34894913G>T	NCBI36
NG_013368.1:g.5661G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448838.8:c.-21+304G>T	ENSP00000389404.3:n.-21+304G>T
ENST00000227868.9:c.135G>T MANE Select	ENSP00000227868.4:p.Trp45Cys
ENST00000227868.8:c.135G>T	ENSP00000227868.4:p.Trp45Cys
ENST00000430469.6:c.135G>T	ENSP00000415695.2:p.Trp45Cys
ENST00000448838.7:c.115+304G>T	ENSP00000389404.2:n.115+304G>T
ENST00000533262.1:c.135G>T	ENSP00000432277.1:p.Trp45Cys
ENST00000533550.5:c.-21+852G>T	ENSP00000431281.1:n.-21+852G>T
NM_001135024.1:c.115+304G>T	NP_001128496.1:n.115+304G>T
NM_001166158.1:c.135G>T	NP_001159630.1:p.Trp45Cys
NM_003477.2:c.135G>T	NP_003468.2:p.Trp45Cys
XM_011520390.1:c.-21+852G>T	XP_011518692.1:n.-21+852G>T
NM_003477.3:c.135G>T MANE Select	NP_003468.2:p.Trp45Cys
NM_001135024.2:c.-21+304G>T	NP_001128496.2:n.-21+304G>T
NM_001166158.2:c.135G>T	NP_001159630.1:p.Trp45Cys