Canonical Allele Identifier: CA654436058

Gene: SDHD

Linked Data

• COSMIC: COSN19633797 ; COSN19644028 ; COSN19651131

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095104_112095105insG , CM000673.2:g.112095104_112095105insG	GRCh38
NC_000011.9:g.111965828_111965829insG , CM000673.1:g.111965828_111965829insG	GRCh37
NC_000011.8:g.111471038_111471039insG	NCBI36
NG_012337.2:g.13258_13259insG
NG_012337.3:g.13258_13259insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*353_*354insG	ENSP00000432946.2:n.*353_*354insG
ENST00000534010.2:c.314+6093_314+6094insG	ENSP00000433202.2:n.314+6093_314+6094insG
ENST00000375549.8:c.*134_*135insG MANE Select	ENSP00000364699.3:n.*134_*135insG
ENST00000528021.6:c.314+6093_314+6094insG	ENSP00000432465.1:n.314+6093_314+6094insG
ENST00000375549.7:c.*134_*135insG	ENSP00000364699.3:n.*134_*135insG
ENST00000525291.5:c.*134_*135insG	ENSP00000436669.1:n.*134_*135insG
ENST00000525987.5:n.319+6093_319+6094insG
ENST00000526592.5:c.*312_*313insG	ENSP00000432005.1:n.*312_*313insG
ENST00000528021.5:c.314+6093_314+6094insG	ENSP00000432465.1:n.314+6093_314+6094insG
ENST00000528048.5:c.*211_*212insG	ENSP00000436217.1:n.*211_*212insG
ENST00000528182.5:c.*211_*212insG	ENSP00000435475.1:n.*211_*212insG
ENST00000530923.5:c.658_659insG
ENST00000531744.5:c.314+6093_314+6094insG	ENSP00000456957.1:n.314+6093_314+6094insG
ENST00000532699.1:c.314+6093_314+6094insG	ENSP00000456434.1:n.314+6093_314+6094insG
ENST00000534010.1:c.145+6093_145+6094insG
NM_001276503.1:c.*211_*212insG	NP_001263432.1:n.*211_*212insG
NM_001276504.1:c.*134_*135insG	NP_001263433.1:n.*134_*135insG
NM_001276506.1:c.*312_*313insG	NP_001263435.1:n.*312_*313insG
NM_003002.3:c.*134_*135insG	NP_002993.1:n.*134_*135insG
NR_077060.1:n.752_753insG
NM_003002.4:c.*134_*135insG MANE Select	NP_002993.1:n.*134_*135insG
NM_001276503.2:c.*211_*212insG	NP_001263432.1:n.*211_*212insG
NM_001276504.2:c.*134_*135insG	NP_001263433.1:n.*134_*135insG
NM_001276506.2:c.*312_*313insG	NP_001263435.1:n.*312_*313insG
NR_077060.2:n.703_704insG