Canonical Allele Identifier: CA2000553797

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094821G= , CM000673.2:g.112094821G=	GRCh38
NC_000011.9:g.111965545G= , CM000673.1:g.111965545G=	GRCh37
NC_000011.8:g.111470755G=	NCBI36
NG_012337.2:g.12975G=
NG_012337.3:g.12975G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*70G=	ENSP00000432946.2:n.*70G=
ENST00000534010.2:c.314+5810G=	ENSP00000433202.2:n.314+5810G=
ENST00000375549.8:c.331G= MANE Select	ENSP00000364699.3:p.Val111=
ENST00000528021.6:c.314+5810G=	ENSP00000432465.1:n.314+5810G=
ENST00000375549.7:c.331G=	ENSP00000364699.3:p.Val111=
ENST00000525291.5:c.214G=	ENSP00000436669.1:p.Val72=
ENST00000525987.5:n.319+5810G=
ENST00000526592.5:c.*29G=	ENSP00000432005.1:n.*29G=
ENST00000528021.5:c.314+5810G=	ENSP00000432465.1:n.314+5810G=
ENST00000528048.5:c.186G=	ENSP00000436217.1:p.Leu62=
ENST00000528182.5:c.324G=	ENSP00000435475.1:p.Leu108=
ENST00000530923.5:c.375G=
ENST00000531744.5:c.314+5810G=	ENSP00000456957.1:n.314+5810G=
ENST00000532699.1:c.314+5810G=	ENSP00000456434.1:n.314+5810G=
ENST00000534010.1:c.145+5810G=
NM_001276503.1:c.186G=	NP_001263432.1:p.Leu62=
NM_001276504.1:c.214G=	NP_001263433.1:p.Val72=
NM_001276506.1:c.*29G=	NP_001263435.1:n.*29G=
NM_003002.3:c.331G=	NP_002993.1:p.Val111=
NR_077060.1:n.469G=
NM_003002.4:c.331G= MANE Select	NP_002993.1:p.Val111=
NM_001276503.2:c.186G=	NP_001263432.1:p.Leu62=
NM_001276504.2:c.214G=	NP_001263433.1:p.Val72=
NM_001276506.2:c.*29G=	NP_001263435.1:n.*29G=
NR_077060.2:n.420G=