Canonical Allele Identifier: CA2418225928

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19360051C= , CM000685.2:g.19360051C=	GRCh38
NC_000023.10:g.19378169C= , CM000685.1:g.19378169C=	GRCh37
NC_000023.9:g.19288090C=	NCBI36
NG_016781.1:g.21159C=
NG_021184.1:g.160211G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*398C=	ENSP00000348062.6:n.*398C=
ENST00000423505.6:c.*398C=	ENSP00000406473.2:n.*398C=
ENST00000696704.1:c.*903C=	ENSP00000512823.1:n.*903C=
ENST00000696705.1:c.*1026C=	ENSP00000512824.1:n.*1026C=
ENST00000422285.7:c.*398C= MANE Select	ENSP00000394382.2:n.*398C=
ENST00000379806.9:c.*398C=	ENSP00000369134.5:n.*398C=
ENST00000422285.6:c.*398C=	ENSP00000394382.2:n.*398C=
ENST00000540249.5:c.*398C=	ENSP00000440761.1:n.*398C=
ENST00000545074.5:c.*398C=	ENSP00000438550.1:n.*398C=
NM_000284.3:c.*398C=	NP_000275.1:n.*398C=
NM_001173454.1:c.*398C=	NP_001166925.1:n.*398C=
NM_001173455.1:c.*398C=	NP_001166926.1:n.*398C=
NM_001173456.1:c.*398C=	NP_001166927.1:n.*398C=
XM_011545531.1:c.*398C=	XP_011543833.1:n.*398C=
XM_011545532.1:c.*398C=	XP_011543834.1:n.*398C=
NM_000284.4:c.*398C= MANE Select	NP_000275.1:n.*398C=
NM_001173454.2:c.*398C=	NP_001166925.1:n.*398C=
NM_001173455.2:c.*398C=	NP_001166926.1:n.*398C=
NM_001173456.2:c.*398C=	NP_001166927.1:n.*398C=