Canonical Allele Identifier: CA343366139

Gene: SDHC

Linked Data

• MyVariant Identifiers: chr1:g.161310442G>C (hg19) ; chr1:g.161340652G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340652G>C , CM000663.2:g.161340652G>C	GRCh38
NC_000001.10:g.161310442G>C , CM000663.1:g.161310442G>C	GRCh37
NC_000001.9:g.159577066G>C	NCBI36
NG_012767.1:g.31277G>C , LRG_317:g.31277G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*239G>C	ENSP00000482902.2:n.*239G>C
ENST00000367975.7:c.238G>C MANE Select	ENSP00000356953.3:p.Ala80Pro
ENST00000342751.8:c.238G>C	ENSP00000356952.3:p.Ala80Pro
ENST00000367975.6:c.238G>C	ENSP00000356953.2:p.Ala80Pro
ENST00000392169.6:c.79G>C	ENSP00000376009.2:p.Ala27Pro
ENST00000432287.6:c.136G>C	ENSP00000390558.2:p.Ala46Pro
ENST00000470743.4:c.336G>C
ENST00000504963.5:c.*61G>C	ENSP00000423929.1:n.*61G>C
ENST00000513009.5:c.136G>C	ENSP00000423260.1:p.Ala46Pro
NM_001035511.1:c.238G>C	NP_001030588.1:p.Ala80Pro
NM_001035512.1:c.136G>C	NP_001030589.1:p.Ala46Pro
NM_001035513.1:c.79G>C	NP_001030590.1:p.Ala27Pro
NM_001278172.1:c.136G>C	NP_001265101.1:p.Ala46Pro
NM_003001.3:c.238G>C , LRG_317t1:c.238G>C	NP_002992.1:p.Ala80Pro
NR_103459.1:n.295G>C
NM_001035511.2:c.238G>C	NP_001030588.1:p.Ala80Pro
NM_001035512.2:c.136G>C	NP_001030589.1:p.Ala46Pro
NM_001035513.2:c.79G>C	NP_001030590.1:p.Ala27Pro
NM_001278172.2:c.136G>C	NP_001265101.1:p.Ala46Pro
NM_003001.5:c.238G>C MANE Select	NP_002992.1:p.Ala80Pro
NR_103459.2:n.290G>C