Canonical Allele Identifier: CA2000554397

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095260T= , CM000673.2:g.112095260T=	GRCh38
NC_000011.9:g.111965984T= , CM000673.1:g.111965984T=	GRCh37
NC_000011.8:g.111471194T=	NCBI36
NG_012337.2:g.13414T=
NG_012337.3:g.13414T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6249T=	ENSP00000433202.2:n.314+6249T=
ENST00000375549.8:c.*290T= MANE Select	ENSP00000364699.3:n.*290T=
ENST00000528021.6:c.314+6249T=	ENSP00000432465.1:n.314+6249T=
ENST00000375549.7:c.*290T=	ENSP00000364699.3:n.*290T=
ENST00000525291.5:c.*290T=	ENSP00000436669.1:n.*290T=
ENST00000525987.5:n.319+6249T=
ENST00000528021.5:c.314+6249T=	ENSP00000432465.1:n.314+6249T=
ENST00000528048.5:c.*367T=	ENSP00000436217.1:n.*367T=
ENST00000531744.5:c.314+6249T=	ENSP00000456957.1:n.314+6249T=
ENST00000532699.1:c.314+6249T=	ENSP00000456434.1:n.314+6249T=
ENST00000534010.1:c.145+6249T=
NM_001276503.1:c.*367T=	NP_001263432.1:n.*367T=
NM_001276504.1:c.*290T=	NP_001263433.1:n.*290T=
NM_001276506.1:c.*468T=	NP_001263435.1:n.*468T=
NM_003002.3:c.*290T=	NP_002993.1:n.*290T=
NR_077060.1:n.908T=
NM_003002.4:c.*290T= MANE Select	NP_002993.1:n.*290T=
NM_001276503.2:c.*367T=	NP_001263432.1:n.*367T=
NM_001276504.2:c.*290T=	NP_001263433.1:n.*290T=
NM_001276506.2:c.*468T=	NP_001263435.1:n.*468T=
NR_077060.2:n.859T=