Canonical Allele Identifier: CA2000554149

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094944_112094953delinsGCTGTTGCCA , CM000673.2:g.112094944_112094953delinsGCTGTTGCCA	GRCh38
NC_000011.9:g.111965668_111965677delinsGCTGTTGCCA , CM000673.1:g.111965668_111965677delinsGCTGTTGCCA	GRCh37
NC_000011.8:g.111470878_111470887delinsGCTGTTGCCA	NCBI36
NG_012337.2:g.13098_13107delinsGCTGTTGCCA
NG_012337.3:g.13098_13107delinsGCTGTTGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*193_*202delinsGCTGTTGCCA	ENSP00000432946.2:n.*193_*202delinsGCTGTTGCCA
ENST00000534010.2:c.314+5933_314+5942delinsGCTGTTGCCA	ENSP00000433202.2:n.314+5933_314+5942delinsGCTGTTGCCA
ENST00000375549.8:c.454_463delinsGCTGTTGCCA MANE Select	ENSP00000364699.3:p.Ala152=
ENST00000528021.6:c.314+5933_314+5942delinsGCTGTTGCCA	ENSP00000432465.1:n.314+5933_314+5942delinsGCTGTTGCCA
ENST00000375549.7:c.454_463delinsGCTGTTGCCA	ENSP00000364699.3:p.Ala152=
ENST00000525291.5:c.337_346delinsGCTGTTGCCA	ENSP00000436669.1:p.Ala113=
ENST00000525987.5:n.319+5933_319+5942delinsGCTGTTGCCA
ENST00000526592.5:c.*152_*161delinsGCTGTTGCCA	ENSP00000432005.1:n.*152_*161delinsGCTGTTGCCA
ENST00000528021.5:c.314+5933_314+5942delinsGCTGTTGCCA	ENSP00000432465.1:n.314+5933_314+5942delinsGCTGTTGCCA
ENST00000528048.5:c.*51_*60delinsGCTGTTGCCA	ENSP00000436217.1:n.*51_*60delinsGCTGTTGCCA
ENST00000528182.5:c.*51_*60delinsGCTGTTGCCA	ENSP00000435475.1:n.*51_*60delinsGCTGTTGCCA
ENST00000530923.5:c.498_507delinsGCTGTTGCCA
ENST00000531744.5:c.314+5933_314+5942delinsGCTGTTGCCA	ENSP00000456957.1:n.314+5933_314+5942delinsGCTGTTGCCA
ENST00000532699.1:c.314+5933_314+5942delinsGCTGTTGCCA	ENSP00000456434.1:n.314+5933_314+5942delinsGCTGTTGCCA
ENST00000534010.1:c.145+5933_145+5942delinsGCTGTTGCCA
NM_001276503.1:c.*51_*60delinsGCTGTTGCCA	NP_001263432.1:n.*51_*60delinsGCTGTTGCCA
NM_001276504.1:c.337_346delinsGCTGTTGCCA	NP_001263433.1:p.Ala113=
NM_001276506.1:c.*152_*161delinsGCTGTTGCCA	NP_001263435.1:n.*152_*161delinsGCTGTTGCCA
NM_003002.3:c.454_463delinsGCTGTTGCCA	NP_002993.1:p.Ala152=
NR_077060.1:n.592_601delinsGCTGTTGCCA
NM_003002.4:c.454_463delinsGCTGTTGCCA MANE Select	NP_002993.1:p.Ala152=
NM_001276503.2:c.*51_*60delinsGCTGTTGCCA	NP_001263432.1:n.*51_*60delinsGCTGTTGCCA
NM_001276504.2:c.337_346delinsGCTGTTGCCA	NP_001263433.1:p.Ala113=
NM_001276506.2:c.*152_*161delinsGCTGTTGCCA	NP_001263435.1:n.*152_*161delinsGCTGTTGCCA
NR_077060.2:n.543_552delinsGCTGTTGCCA