Canonical Allele Identifier: CA1140716590

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161357094_161357095delinsTT , CM000663.2:g.161357094_161357095delinsTT	GRCh38
NC_000001.10:g.161326884_161326885delinsTT , CM000663.1:g.161326884_161326885delinsTT	GRCh37
NC_000001.9:g.159593508_159593509delinsTT	NCBI36
NG_012767.1:g.47719_47720delinsTT , LRG_317:g.47719_47720delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*406+254_*406+255delinsTT	ENSP00000482902.2:n.*406+254_*406+255delinsTT
ENST00000367975.7:c.405+254_405+255delinsTT MANE Select	ENSP00000356953.3:n.405+254_405+255delinsTT
ENST00000342751.8:c.242-5235_242-5234delinsTT	ENSP00000356952.3:n.242-5235_242-5234delinsTT
ENST00000367975.6:c.405+254_405+255delinsTT	ENSP00000356953.2:n.405+254_405+255delinsTT
ENST00000392169.6:c.246+254_246+255delinsTT	ENSP00000376009.2:n.246+254_246+255delinsTT
ENST00000432287.6:c.303+254_303+255delinsTT	ENSP00000390558.2:n.303+254_303+255delinsTT
ENST00000470743.4:c.503+254_503+255delinsTT
ENST00000504963.5:c.*228+254_*228+255delinsTT	ENSP00000423929.1:n.*228+254_*228+255delinsTT
ENST00000513009.5:c.140-5235_140-5234delinsTT	ENSP00000423260.1:n.140-5235_140-5234delinsTT
NM_001035511.1:c.242-5235_242-5234delinsTT	NP_001030588.1:n.242-5235_242-5234delinsTT
NM_001035512.1:c.303+254_303+255delinsTT	NP_001030589.1:n.303+254_303+255delinsTT
NM_001035513.1:c.246+254_246+255delinsTT	NP_001030590.1:n.246+254_246+255delinsTT
NM_001278172.1:c.140-5235_140-5234delinsTT	NP_001265101.1:n.140-5235_140-5234delinsTT
NM_003001.3:c.405+254_405+255delinsTT , LRG_317t1:c.405+254_405+255delinsTT	NP_002992.1:n.405+254_405+255delinsTT
NR_103459.1:n.462+254_462+255delinsTT
NM_001035511.2:c.242-5235_242-5234delinsTT	NP_001030588.1:n.242-5235_242-5234delinsTT
NM_001035512.2:c.303+254_303+255delinsTT	NP_001030589.1:n.303+254_303+255delinsTT
NM_001035513.2:c.246+254_246+255delinsTT	NP_001030590.1:n.246+254_246+255delinsTT
NM_001278172.2:c.140-5235_140-5234delinsTT	NP_001265101.1:n.140-5235_140-5234delinsTT
NM_003001.5:c.405+254_405+255delinsTT MANE Select	NP_002992.1:n.405+254_405+255delinsTT
NR_103459.2:n.457+254_457+255delinsTT