Canonical Allele Identifier: CA1210299

Gene: SDHC

Linked Data

• dbSNP Id: rs780547446
• ExAC: 1:161310359 ATTGTCT / A
• gnomAD v2: 1-161310359-ATTGTCT-A
• gnomAD v4: 1-161340569-ATTGTCT-A
• MyVariant Identifiers: chr1:g.161310360_161310365del (hg19) ; chr1:g.161340570_161340575del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340574_161340579del , CM000663.2:g.161340574_161340579del	GRCh38
NC_000001.10:g.161310364_161310369del , CM000663.1:g.161310364_161310369del	GRCh37
NC_000001.9:g.159576988_159576993del	NCBI36
NG_012767.1:g.31199_31204del , LRG_317:g.31199_31204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*181-20_*181-15del	ENSP00000482902.2:n.*181-20_*181-15del
ENST00000367975.7:c.180-20_180-15del MANE Select	ENSP00000356953.3:n.180-20_180-15del
ENST00000342751.8:c.180-20_180-15del	ENSP00000356952.3:n.180-20_180-15del
ENST00000367975.6:c.180-20_180-15del	ENSP00000356953.2:n.180-20_180-15del
ENST00000392169.6:c.21-20_21-15del	ENSP00000376009.2:n.21-20_21-15del
ENST00000432287.6:c.78-20_78-15del	ENSP00000390558.2:n.78-20_78-15del
ENST00000470743.4:c.278-20_278-15del
ENST00000504963.5:c.*3-20_*3-15del	ENSP00000423929.1:n.*3-20_*3-15del
ENST00000513009.5:c.78-20_78-15del	ENSP00000423260.1:n.78-20_78-15del
NM_001035511.1:c.180-20_180-15del	NP_001030588.1:n.180-20_180-15del
NM_001035512.1:c.78-20_78-15del	NP_001030589.1:n.78-20_78-15del
NM_001035513.1:c.21-20_21-15del	NP_001030590.1:n.21-20_21-15del
NM_001278172.1:c.78-20_78-15del	NP_001265101.1:n.78-20_78-15del
NM_003001.3:c.180-20_180-15del , LRG_317t1:c.180-20_180-15del	NP_002992.1:n.180-20_180-15del
NR_103459.1:n.237-20_237-15del
NM_001035511.2:c.180-20_180-15del	NP_001030588.1:n.180-20_180-15del
NM_001035512.2:c.78-20_78-15del	NP_001030589.1:n.78-20_78-15del
NM_001035513.2:c.21-20_21-15del	NP_001030590.1:n.21-20_21-15del
NM_001278172.2:c.78-20_78-15del	NP_001265101.1:n.78-20_78-15del
NM_003001.5:c.180-20_180-15del MANE Select	NP_002992.1:n.180-20_180-15del
NR_103459.2:n.232-20_232-15del