Canonical Allele Identifier: CA2000553631

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094762_112094764delinsCTG , CM000673.2:g.112094762_112094764delinsCTG	GRCh38
NC_000011.9:g.111965486_111965488delinsCTG , CM000673.1:g.111965486_111965488delinsCTG	GRCh37
NC_000011.8:g.111470696_111470698delinsCTG	NCBI36
NG_012337.2:g.12916_12918delinsCTG
NG_012337.3:g.12916_12918delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*54-43_*54-41delinsCTG	ENSP00000432946.2:n.*54-43_*54-41delinsCT...
ENST00000534010.2:c.314+5751_314+5753delinsCTG	ENSP00000433202.2:n.314+5751_314+5753deli...
ENST00000375549.8:c.315-43_315-41delinsCTG MANE Select	ENSP00000364699.3:n.315-43_315-41delinsCT...
ENST00000528021.6:c.314+5751_314+5753delinsCTG	ENSP00000432465.1:n.314+5751_314+5753deli...
ENST00000375549.7:c.315-43_315-41delinsCTG	ENSP00000364699.3:n.315-43_315-41delinsCT...
ENST00000525291.5:c.198-43_198-41delinsCTG	ENSP00000436669.1:n.198-43_198-41delinsCT...
ENST00000525987.5:n.319+5751_319+5753delinsCTG
ENST00000526592.5:c.*13-43_*13-41delinsCTG	ENSP00000432005.1:n.*13-43_*13-41delinsCT...
ENST00000528021.5:c.314+5751_314+5753delinsCTG	ENSP00000432465.1:n.314+5751_314+5753deli...
ENST00000528048.5:c.170-43_170-41delinsCTG	ENSP00000436217.1:n.170-43_170-41delinsCT...
ENST00000528182.5:c.308-43_308-41delinsCTG	ENSP00000435475.1:n.308-43_308-41delinsCT...
ENST00000530923.5:c.359-43_359-41delinsCTG
ENST00000531744.5:c.314+5751_314+5753delinsCTG	ENSP00000456957.1:n.314+5751_314+5753deli...
ENST00000532699.1:c.314+5751_314+5753delinsCTG	ENSP00000456434.1:n.314+5751_314+5753deli...
ENST00000534010.1:c.145+5751_145+5753delinsCTG
NM_001276503.1:c.170-43_170-41delinsCTG	NP_001263432.1:n.170-43_170-41delinsCTG
NM_001276504.1:c.198-43_198-41delinsCTG	NP_001263433.1:n.198-43_198-41delinsCTG
NM_001276506.1:c.*13-43_*13-41delinsCTG	NP_001263435.1:n.*13-43_*13-41delinsCTG
NM_003002.3:c.315-43_315-41delinsCTG	NP_002993.1:n.315-43_315-41delinsCTG
NR_077060.1:n.453-43_453-41delinsCTG
NM_003002.4:c.315-43_315-41delinsCTG MANE Select	NP_002993.1:n.315-43_315-41delinsCTG
NM_001276503.2:c.170-43_170-41delinsCTG	NP_001263432.1:n.170-43_170-41delinsCTG
NM_001276504.2:c.198-43_198-41delinsCTG	NP_001263433.1:n.198-43_198-41delinsCTG
NM_001276506.2:c.*13-43_*13-41delinsCTG	NP_001263435.1:n.*13-43_*13-41delinsCTG
NR_077060.2:n.404-43_404-41delinsCTG