Canonical Allele Identifier: CA2000553793

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094818G= , CM000673.2:g.112094818G=	GRCh38
NC_000011.9:g.111965542G= , CM000673.1:g.111965542G=	GRCh37
NC_000011.8:g.111470752G=	NCBI36
NG_012337.2:g.12972G=
NG_012337.3:g.12972G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*67G=	ENSP00000432946.2:n.*67G=
ENST00000534010.2:c.314+5807G=	ENSP00000433202.2:n.314+5807G=
ENST00000375549.8:c.328G= MANE Select	ENSP00000364699.3:p.Val110=
ENST00000528021.6:c.314+5807G=	ENSP00000432465.1:n.314+5807G=
ENST00000375549.7:c.328G=	ENSP00000364699.3:p.Val110=
ENST00000525291.5:c.211G=	ENSP00000436669.1:p.Val71=
ENST00000525987.5:n.319+5807G=
ENST00000526592.5:c.*26G=	ENSP00000432005.1:n.*26G=
ENST00000528021.5:c.314+5807G=	ENSP00000432465.1:n.314+5807G=
ENST00000528048.5:c.183G=	ENSP00000436217.1:p.Lys61=
ENST00000528182.5:c.321G=	ENSP00000435475.1:p.Lys107=
ENST00000530923.5:c.372G=
ENST00000531744.5:c.314+5807G=	ENSP00000456957.1:n.314+5807G=
ENST00000532699.1:c.314+5807G=	ENSP00000456434.1:n.314+5807G=
ENST00000534010.1:c.145+5807G=
NM_001276503.1:c.183G=	NP_001263432.1:p.Lys61=
NM_001276504.1:c.211G=	NP_001263433.1:p.Val71=
NM_001276506.1:c.*26G=	NP_001263435.1:n.*26G=
NM_003002.3:c.328G=	NP_002993.1:p.Val110=
NR_077060.1:n.466G=
NM_003002.4:c.328G= MANE Select	NP_002993.1:p.Val110=
NM_001276503.2:c.183G=	NP_001263432.1:p.Lys61=
NM_001276504.2:c.211G=	NP_001263433.1:p.Val71=
NM_001276506.2:c.*26G=	NP_001263435.1:n.*26G=
NR_077060.2:n.417G=