Canonical Allele Identifier: CA2000554433

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095292C= , CM000673.2:g.112095292C=	GRCh38
NC_000011.9:g.111966016C= , CM000673.1:g.111966016C=	GRCh37
NC_000011.8:g.111471226C=	NCBI36
NG_012337.2:g.13446C=
NG_012337.3:g.13446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6281C=	ENSP00000433202.2:n.314+6281C=
ENST00000375549.8:c.*322C= MANE Select	ENSP00000364699.3:n.*322C=
ENST00000528021.6:c.314+6281C=	ENSP00000432465.1:n.314+6281C=
ENST00000375549.7:c.*322C=	ENSP00000364699.3:n.*322C=
ENST00000525291.5:c.*322C=	ENSP00000436669.1:n.*322C=
ENST00000525987.5:n.319+6281C=
ENST00000528021.5:c.314+6281C=	ENSP00000432465.1:n.314+6281C=
ENST00000528048.5:c.*399C=	ENSP00000436217.1:n.*399C=
ENST00000531744.5:c.314+6281C=	ENSP00000456957.1:n.314+6281C=
ENST00000532699.1:c.314+6281C=	ENSP00000456434.1:n.314+6281C=
ENST00000534010.1:c.145+6281C=
NM_001276503.1:c.*399C=	NP_001263432.1:n.*399C=
NM_001276504.1:c.*322C=	NP_001263433.1:n.*322C=
NM_001276506.1:c.*500C=	NP_001263435.1:n.*500C=
NM_003002.3:c.*322C=	NP_002993.1:n.*322C=
NR_077060.1:n.940C=
NM_003002.4:c.*322C= MANE Select	NP_002993.1:n.*322C=
NM_001276503.2:c.*399C=	NP_001263432.1:n.*399C=
NM_001276504.2:c.*322C=	NP_001263433.1:n.*322C=
NM_001276506.2:c.*500C=	NP_001263435.1:n.*500C=
NR_077060.2:n.891C=