Canonical Allele Identifier: CA2000553969

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094866G= , CM000673.2:g.112094866G=	GRCh38
NC_000011.9:g.111965590G= , CM000673.1:g.111965590G=	GRCh37
NC_000011.8:g.111470800G=	NCBI36
NG_012337.2:g.13020G=
NG_012337.3:g.13020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*115G=	ENSP00000432946.2:n.*115G=
ENST00000534010.2:c.314+5855G=	ENSP00000433202.2:n.314+5855G=
ENST00000375549.8:c.376G= MANE Select	ENSP00000364699.3:p.Ala126=
ENST00000528021.6:c.314+5855G=	ENSP00000432465.1:n.314+5855G=
ENST00000375549.7:c.376G=	ENSP00000364699.3:p.Ala126=
ENST00000525291.5:c.259G=	ENSP00000436669.1:p.Ala87=
ENST00000525987.5:n.319+5855G=
ENST00000526592.5:c.*74G=	ENSP00000432005.1:n.*74G=
ENST00000528021.5:c.314+5855G=	ENSP00000432465.1:n.314+5855G=
ENST00000528048.5:c.231G=	ENSP00000436217.1:p.Arg77=
ENST00000528182.5:c.369G=	ENSP00000435475.1:p.Arg123=
ENST00000530923.5:c.420G=
ENST00000531744.5:c.314+5855G=	ENSP00000456957.1:n.314+5855G=
ENST00000532699.1:c.314+5855G=	ENSP00000456434.1:n.314+5855G=
ENST00000534010.1:c.145+5855G=
NM_001276503.1:c.231G=	NP_001263432.1:p.Arg77=
NM_001276504.1:c.259G=	NP_001263433.1:p.Ala87=
NM_001276506.1:c.*74G=	NP_001263435.1:n.*74G=
NM_003002.3:c.376G=	NP_002993.1:p.Ala126=
NR_077060.1:n.514G=
NM_003002.4:c.376G= MANE Select	NP_002993.1:p.Ala126=
NM_001276503.2:c.231G=	NP_001263432.1:p.Arg77=
NM_001276504.2:c.259G=	NP_001263433.1:p.Ala87=
NM_001276506.2:c.*74G=	NP_001263435.1:n.*74G=
NR_077060.2:n.465G=