Canonical Allele Identifier: CA2000554446

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095303T= , CM000673.2:g.112095303T=	GRCh38
NC_000011.9:g.111966027T= , CM000673.1:g.111966027T=	GRCh37
NC_000011.8:g.111471237T=	NCBI36
NG_012337.2:g.13457T=
NG_012337.3:g.13457T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6292T=	ENSP00000433202.2:n.314+6292T=
ENST00000375549.8:c.*333T= MANE Select	ENSP00000364699.3:n.*333T=
ENST00000528021.6:c.314+6292T=	ENSP00000432465.1:n.314+6292T=
ENST00000375549.7:c.*333T=	ENSP00000364699.3:n.*333T=
ENST00000525291.5:c.*333T=	ENSP00000436669.1:n.*333T=
ENST00000525987.5:n.319+6292T=
ENST00000528021.5:c.314+6292T=	ENSP00000432465.1:n.314+6292T=
ENST00000528048.5:c.*410T=	ENSP00000436217.1:n.*410T=
ENST00000531744.5:c.314+6292T=	ENSP00000456957.1:n.314+6292T=
ENST00000532699.1:c.314+6292T=	ENSP00000456434.1:n.314+6292T=
ENST00000534010.1:c.145+6292T=
NM_001276503.1:c.*410T=	NP_001263432.1:n.*410T=
NM_001276504.1:c.*333T=	NP_001263433.1:n.*333T=
NM_001276506.1:c.*511T=	NP_001263435.1:n.*511T=
NM_003002.3:c.*333T=	NP_002993.1:n.*333T=
NR_077060.1:n.951T=
NM_003002.4:c.*333T= MANE Select	NP_002993.1:n.*333T=
NM_001276503.2:c.*410T=	NP_001263432.1:n.*410T=
NM_001276504.2:c.*333T=	NP_001263433.1:n.*333T=
NM_001276506.2:c.*511T=	NP_001263435.1:n.*511T=
NR_077060.2:n.902T=