Canonical Allele Identifier: CA2000554165

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094950G= , CM000673.2:g.112094950G=	GRCh38
NC_000011.9:g.111965674G= , CM000673.1:g.111965674G=	GRCh37
NC_000011.8:g.111470884G=	NCBI36
NG_012337.2:g.13104G=
NG_012337.3:g.13104G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*199G=	ENSP00000432946.2:n.*199G=
ENST00000534010.2:c.314+5939G=	ENSP00000433202.2:n.314+5939G=
ENST00000375549.8:c.460G= MANE Select	ENSP00000364699.3:p.Ala154=
ENST00000528021.6:c.314+5939G=	ENSP00000432465.1:n.314+5939G=
ENST00000375549.7:c.460G=	ENSP00000364699.3:p.Ala154=
ENST00000525291.5:c.343G=	ENSP00000436669.1:p.Ala115=
ENST00000525987.5:n.319+5939G=
ENST00000526592.5:c.*158G=	ENSP00000432005.1:n.*158G=
ENST00000528021.5:c.314+5939G=	ENSP00000432465.1:n.314+5939G=
ENST00000528048.5:c.*57G=	ENSP00000436217.1:n.*57G=
ENST00000528182.5:c.*57G=	ENSP00000435475.1:n.*57G=
ENST00000530923.5:c.504G=
ENST00000531744.5:c.314+5939G=	ENSP00000456957.1:n.314+5939G=
ENST00000532699.1:c.314+5939G=	ENSP00000456434.1:n.314+5939G=
ENST00000534010.1:c.145+5939G=
NM_001276503.1:c.*57G=	NP_001263432.1:n.*57G=
NM_001276504.1:c.343G=	NP_001263433.1:p.Ala115=
NM_001276506.1:c.*158G=	NP_001263435.1:n.*158G=
NM_003002.3:c.460G=	NP_002993.1:p.Ala154=
NR_077060.1:n.598G=
NM_003002.4:c.460G= MANE Select	NP_002993.1:p.Ala154=
NM_001276503.2:c.*57G=	NP_001263432.1:n.*57G=
NM_001276504.2:c.343G=	NP_001263433.1:p.Ala115=
NM_001276506.2:c.*158G=	NP_001263435.1:n.*158G=
NR_077060.2:n.549G=