Canonical Allele Identifier: CA2793647970

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095212C>G , CM000673.2:g.112095212C>G	GRCh38
NC_000011.9:g.111965936C>G , CM000673.1:g.111965936C>G	GRCh37
NC_000011.8:g.111471146C>G	NCBI36
NG_012337.2:g.13366C>G
NG_012337.3:g.13366C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6201C>G	ENSP00000433202.2:n.314+6201C>G
ENST00000375549.8:c.*242C>G MANE Select	ENSP00000364699.3:n.*242C>G
ENST00000528021.6:c.314+6201C>G	ENSP00000432465.1:n.314+6201C>G
ENST00000375549.7:c.*242C>G	ENSP00000364699.3:n.*242C>G
ENST00000525291.5:c.*242C>G	ENSP00000436669.1:n.*242C>G
ENST00000525987.5:n.319+6201C>G
ENST00000526592.5:c.*420C>G	ENSP00000432005.1:n.*420C>G
ENST00000528021.5:c.314+6201C>G	ENSP00000432465.1:n.314+6201C>G
ENST00000528048.5:c.*319C>G	ENSP00000436217.1:n.*319C>G
ENST00000528182.5:c.*319C>G	ENSP00000435475.1:n.*319C>G
ENST00000531744.5:c.314+6201C>G	ENSP00000456957.1:n.314+6201C>G
ENST00000532699.1:c.314+6201C>G	ENSP00000456434.1:n.314+6201C>G
ENST00000534010.1:c.145+6201C>G
NM_001276503.1:c.*319C>G	NP_001263432.1:n.*319C>G
NM_001276504.1:c.*242C>G	NP_001263433.1:n.*242C>G
NM_001276506.1:c.*420C>G	NP_001263435.1:n.*420C>G
NM_003002.3:c.*242C>G	NP_002993.1:n.*242C>G
NR_077060.1:n.860C>G
NM_003002.4:c.*242C>G MANE Select	NP_002993.1:n.*242C>G
NM_001276503.2:c.*319C>G	NP_001263432.1:n.*319C>G
NM_001276504.2:c.*242C>G	NP_001263433.1:n.*242C>G
NM_001276506.2:c.*420C>G	NP_001263435.1:n.*420C>G
NR_077060.2:n.811C>G