Canonical Allele Identifier: CA2648775579

Gene: SDHC

Linked Data

• gnomAD v4: 1-161328304-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328304G>A , CM000663.2:g.161328304G>A	GRCh38
NC_000001.10:g.161298094G>A , CM000663.1:g.161298094G>A	GRCh37
NC_000001.9:g.159564718G>A	NCBI36
NG_012767.1:g.18929G>A , LRG_317:g.18929G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*79-92G>A	ENSP00000482902.2:n.*79-92G>A
ENST00000367975.7:c.78-92G>A MANE Select	ENSP00000356953.3:n.78-92G>A
ENST00000342751.8:c.78-92G>A	ENSP00000356952.3:n.78-92G>A
ENST00000367975.6:c.78-92G>A	ENSP00000356953.2:n.78-92G>A
ENST00000392169.6:c.21-12290G>A	ENSP00000376009.2:n.21-12290G>A
ENST00000432287.6:c.77+4634G>A	ENSP00000390558.2:n.77+4634G>A
ENST00000470743.4:c.176-92G>A
ENST00000504963.5:c.78-92G>A	ENSP00000423929.1:n.78-92G>A
ENST00000513009.5:c.77+4634G>A	ENSP00000423260.1:n.77+4634G>A
ENST00000515731.1:n.552-92G>A
NM_001035511.1:c.78-92G>A	NP_001030588.1:n.78-92G>A
NM_001035512.1:c.77+4634G>A	NP_001030589.1:n.77+4634G>A
NM_001035513.1:c.21-12290G>A	NP_001030590.1:n.21-12290G>A
NM_001278172.1:c.77+4634G>A	NP_001265101.1:n.77+4634G>A
NM_003001.3:c.78-92G>A , LRG_317t1:c.78-92G>A	NP_002992.1:n.78-92G>A
NR_103459.1:n.108-92G>A
NM_001035511.2:c.78-92G>A	NP_001030588.1:n.78-92G>A
NM_001035512.2:c.77+4634G>A	NP_001030589.1:n.77+4634G>A
NM_001035513.2:c.21-12290G>A	NP_001030590.1:n.21-12290G>A
NM_001278172.2:c.77+4634G>A	NP_001265101.1:n.77+4634G>A
NM_003001.5:c.78-92G>A MANE Select	NP_002992.1:n.78-92G>A
NR_103459.2:n.103-92G>A