Canonical Allele Identifier: CA2648776172

Gene: SDHC

Linked Data

• gnomAD v4: 1-161340554-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340558del , CM000663.2:g.161340558del	GRCh38
NC_000001.10:g.161310348del , CM000663.1:g.161310348del	GRCh37
NC_000001.9:g.159576972del	NCBI36
NG_012767.1:g.31183del , LRG_317:g.31183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*181-36del	ENSP00000482902.2:n.*181-36del
ENST00000367975.7:c.180-36del MANE Select	ENSP00000356953.3:n.180-36del
ENST00000342751.8:c.180-36del	ENSP00000356952.3:n.180-36del
ENST00000367975.6:c.180-36del	ENSP00000356953.2:n.180-36del
ENST00000392169.6:c.21-36del	ENSP00000376009.2:n.21-36del
ENST00000432287.6:c.78-36del	ENSP00000390558.2:n.78-36del
ENST00000470743.4:c.278-36del
ENST00000504963.5:c.*3-36del	ENSP00000423929.1:n.*3-36del
ENST00000513009.5:c.78-36del	ENSP00000423260.1:n.78-36del
NM_001035511.1:c.180-36del	NP_001030588.1:n.180-36del
NM_001035512.1:c.78-36del	NP_001030589.1:n.78-36del
NM_001035513.1:c.21-36del	NP_001030590.1:n.21-36del
NM_001278172.1:c.78-36del	NP_001265101.1:n.78-36del
NM_003001.3:c.180-36del , LRG_317t1:c.180-36del	NP_002992.1:n.180-36del
NR_103459.1:n.237-36del
NM_001035511.2:c.180-36del	NP_001030588.1:n.180-36del
NM_001035512.2:c.78-36del	NP_001030589.1:n.78-36del
NM_001035513.2:c.21-36del	NP_001030590.1:n.21-36del
NM_001278172.2:c.78-36del	NP_001265101.1:n.78-36del
NM_003001.5:c.180-36del MANE Select	NP_002992.1:n.180-36del
NR_103459.2:n.232-36del