Canonical Allele Identifier: CA2000554379

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095250_112095251delinsGC , CM000673.2:g.112095250_112095251delinsGC	GRCh38
NC_000011.9:g.111965974_111965975delinsGC , CM000673.1:g.111965974_111965975delinsGC	GRCh37
NC_000011.8:g.111471184_111471185delinsGC	NCBI36
NG_012337.2:g.13404_13405delinsGC
NG_012337.3:g.13404_13405delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6239_314+6240delinsGC	ENSP00000433202.2:n.314+6239_314+6240delinsGC
ENST00000375549.8:c.*280_*281delinsGC MANE Select	ENSP00000364699.3:n.*280_*281delinsGC
ENST00000528021.6:c.314+6239_314+6240delinsGC	ENSP00000432465.1:n.314+6239_314+6240delinsGC
ENST00000375549.7:c.*280_*281delinsGC	ENSP00000364699.3:n.*280_*281delinsGC
ENST00000525291.5:c.*280_*281delinsGC	ENSP00000436669.1:n.*280_*281delinsGC
ENST00000525987.5:n.319+6239_319+6240delinsGC
ENST00000528021.5:c.314+6239_314+6240delinsGC	ENSP00000432465.1:n.314+6239_314+6240delinsGC
ENST00000528048.5:c.*357_*358delinsGC	ENSP00000436217.1:n.*357_*358delinsGC
ENST00000531744.5:c.314+6239_314+6240delinsGC	ENSP00000456957.1:n.314+6239_314+6240delinsGC
ENST00000532699.1:c.314+6239_314+6240delinsGC	ENSP00000456434.1:n.314+6239_314+6240delinsGC
ENST00000534010.1:c.145+6239_145+6240delinsGC
NM_001276503.1:c.*357_*358delinsGC	NP_001263432.1:n.*357_*358delinsGC
NM_001276504.1:c.*280_*281delinsGC	NP_001263433.1:n.*280_*281delinsGC
NM_001276506.1:c.*458_*459delinsGC	NP_001263435.1:n.*458_*459delinsGC
NM_003002.3:c.*280_*281delinsGC	NP_002993.1:n.*280_*281delinsGC
NR_077060.1:n.898_899delinsGC
NM_003002.4:c.*280_*281delinsGC MANE Select	NP_002993.1:n.*280_*281delinsGC
NM_001276503.2:c.*357_*358delinsGC	NP_001263432.1:n.*357_*358delinsGC
NM_001276504.2:c.*280_*281delinsGC	NP_001263433.1:n.*280_*281delinsGC
NM_001276506.2:c.*458_*459delinsGC	NP_001263435.1:n.*458_*459delinsGC
NR_077060.2:n.849_850delinsGC