Canonical Allele Identifier: CA2539559026

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095085T>G , CM000673.2:g.112095085T>G	GRCh38
NC_000011.9:g.111965809T>G , CM000673.1:g.111965809T>G	GRCh37
NC_000011.8:g.111471019T>G	NCBI36
NG_012337.2:g.13239T>G
NG_012337.3:g.13239T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*334T>G	ENSP00000432946.2:n.*334T>G
ENST00000534010.2:c.314+6074T>G	ENSP00000433202.2:n.314+6074T>G
ENST00000375549.8:c.*115T>G MANE Select	ENSP00000364699.3:n.*115T>G
ENST00000528021.6:c.314+6074T>G	ENSP00000432465.1:n.314+6074T>G
ENST00000375549.7:c.*115T>G	ENSP00000364699.3:n.*115T>G
ENST00000525291.5:c.*115T>G	ENSP00000436669.1:n.*115T>G
ENST00000525987.5:n.319+6074T>G
ENST00000526592.5:c.*293T>G	ENSP00000432005.1:n.*293T>G
ENST00000528021.5:c.314+6074T>G	ENSP00000432465.1:n.314+6074T>G
ENST00000528048.5:c.*192T>G	ENSP00000436217.1:n.*192T>G
ENST00000528182.5:c.*192T>G	ENSP00000435475.1:n.*192T>G
ENST00000530923.5:c.639T>G
ENST00000531744.5:c.314+6074T>G	ENSP00000456957.1:n.314+6074T>G
ENST00000532699.1:c.314+6074T>G	ENSP00000456434.1:n.314+6074T>G
ENST00000534010.1:c.145+6074T>G
NM_001276503.1:c.*192T>G	NP_001263432.1:n.*192T>G
NM_001276504.1:c.*115T>G	NP_001263433.1:n.*115T>G
NM_001276506.1:c.*293T>G	NP_001263435.1:n.*293T>G
NM_003002.3:c.*115T>G	NP_002993.1:n.*115T>G
NR_077060.1:n.733T>G
NM_003002.4:c.*115T>G MANE Select	NP_002993.1:n.*115T>G
NM_001276503.2:c.*192T>G	NP_001263432.1:n.*192T>G
NM_001276504.2:c.*115T>G	NP_001263433.1:n.*115T>G
NM_001276506.2:c.*293T>G	NP_001263435.1:n.*293T>G
NR_077060.2:n.684T>G