Canonical Allele Identifier: CA1202701878

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340734C= , CM000663.2:g.161340734C=	GRCh38
NC_000001.10:g.161310524C= , CM000663.1:g.161310524C=	GRCh37
NC_000001.9:g.159577148C=	NCBI36
NG_012767.1:g.31359C= , LRG_317:g.31359C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*242+79C=	ENSP00000482902.2:n.*242+79C=
ENST00000367975.7:c.241+79C= MANE Select	ENSP00000356953.3:n.241+79C=
ENST00000342751.8:c.241+79C=	ENSP00000356952.3:n.241+79C=
ENST00000367975.6:c.241+79C=	ENSP00000356953.2:n.241+79C=
ENST00000392169.6:c.82+79C=	ENSP00000376009.2:n.82+79C=
ENST00000432287.6:c.139+79C=	ENSP00000390558.2:n.139+79C=
ENST00000470743.4:c.339+79C=
ENST00000504963.5:c.*64+79C=	ENSP00000423929.1:n.*64+79C=
ENST00000513009.5:c.139+79C=	ENSP00000423260.1:n.139+79C=
NM_001035511.1:c.241+79C=	NP_001030588.1:n.241+79C=
NM_001035512.1:c.139+79C=	NP_001030589.1:n.139+79C=
NM_001035513.1:c.82+79C=	NP_001030590.1:n.82+79C=
NM_001278172.1:c.139+79C=	NP_001265101.1:n.139+79C=
NM_003001.3:c.241+79C= , LRG_317t1:c.241+79C=	NP_002992.1:n.241+79C=
NR_103459.1:n.298+79C=
NM_001035511.2:c.241+79C=	NP_001030588.1:n.241+79C=
NM_001035512.2:c.139+79C=	NP_001030589.1:n.139+79C=
NM_001035513.2:c.82+79C=	NP_001030590.1:n.82+79C=
NM_001278172.2:c.139+79C=	NP_001265101.1:n.139+79C=
NM_003001.5:c.241+79C= MANE Select	NP_002992.1:n.241+79C=
NR_103459.2:n.293+79C=