Canonical Allele Identifier: CA2000553771

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094815_112094817delinsCAA , CM000673.2:g.112094815_112094817delinsCAA	GRCh38
NC_000011.9:g.111965539_111965541delinsCAA , CM000673.1:g.111965539_111965541delinsCAA	GRCh37
NC_000011.8:g.111470749_111470751delinsCAA	NCBI36
NG_012337.2:g.12969_12971delinsCAA
NG_012337.3:g.12969_12971delinsCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*64_*66delinsCAA	ENSP00000432946.2:n.*64_*66delinsCAA
ENST00000534010.2:c.314+5804_314+5806delinsCAA	ENSP00000433202.2:n.314+5804_314+5806delinsCAA
ENST00000375549.8:c.325_327delinsCAA MANE Select	ENSP00000364699.3:p.Gln109=
ENST00000528021.6:c.314+5804_314+5806delinsCAA	ENSP00000432465.1:n.314+5804_314+5806delinsCAA
ENST00000375549.7:c.325_327delinsCAA	ENSP00000364699.3:p.Gln109=
ENST00000525291.5:c.208_210delinsCAA	ENSP00000436669.1:p.Gln70=
ENST00000525987.5:n.319+5804_319+5806delinsCAA
ENST00000526592.5:c.*23_*25delinsCAA	ENSP00000432005.1:n.*23_*25delinsCAA
ENST00000528021.5:c.314+5804_314+5806delinsCAA	ENSP00000432465.1:n.314+5804_314+5806delinsCAA
ENST00000528048.5:c.180_182delinsCAA	ENSP00000436217.1:p.Asp60=
ENST00000528182.5:c.318_320delinsCAA	ENSP00000435475.1:p.Asp106=
ENST00000530923.5:c.369_371delinsCAA
ENST00000531744.5:c.314+5804_314+5806delinsCAA	ENSP00000456957.1:n.314+5804_314+5806delinsCAA
ENST00000532699.1:c.314+5804_314+5806delinsCAA	ENSP00000456434.1:n.314+5804_314+5806delinsCAA
ENST00000534010.1:c.145+5804_145+5806delinsCAA
NM_001276503.1:c.180_182delinsCAA	NP_001263432.1:p.Asp60=
NM_001276504.1:c.208_210delinsCAA	NP_001263433.1:p.Gln70=
NM_001276506.1:c.*23_*25delinsCAA	NP_001263435.1:n.*23_*25delinsCAA
NM_003002.3:c.325_327delinsCAA	NP_002993.1:p.Gln109=
NR_077060.1:n.463_465delinsCAA
NM_003002.4:c.325_327delinsCAA MANE Select	NP_002993.1:p.Gln109=
NM_001276503.2:c.180_182delinsCAA	NP_001263432.1:p.Asp60=
NM_001276504.2:c.208_210delinsCAA	NP_001263433.1:p.Gln70=
NM_001276506.2:c.*23_*25delinsCAA	NP_001263435.1:n.*23_*25delinsCAA
NR_077060.2:n.414_416delinsCAA