Canonical Allele Identifier: CA2697464543
Gene: SDHC HGNC NCBI

Linked Data

dbSNP Id: rs2102335823

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161340547del , CM000663.2:g.161340547del GRCh38
NC_000001.10:g.161310337del , CM000663.1:g.161310337del GRCh37
NC_000001.9:g.159576961del NCBI36
NG_012767.1:g.31172del , LRG_317:g.31172del

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.*181-47del ENSP00000482902.2:n.*181-47del
ENST00000367975.7:c.180-47del MANE Select ENSP00000356953.3:n.180-47del
ENST00000342751.8:c.180-47del ENSP00000356952.3:n.180-47del
ENST00000367975.6:c.180-47del ENSP00000356953.2:n.180-47del
ENST00000392169.6:c.21-47del ENSP00000376009.2:n.21-47del
ENST00000432287.6:c.78-47del ENSP00000390558.2:n.78-47del
ENST00000470743.4:c.278-47del
ENST00000504963.5:c.*3-47del ENSP00000423929.1:n.*3-47del
ENST00000513009.5:c.78-47del ENSP00000423260.1:n.78-47del
NM_001035511.1:c.180-47del NP_001030588.1:n.180-47del
NM_001035512.1:c.78-47del NP_001030589.1:n.78-47del
NM_001035513.1:c.21-47del NP_001030590.1:n.21-47del
NM_001278172.1:c.78-47del NP_001265101.1:n.78-47del
NM_003001.3:c.180-47del , LRG_317t1:c.180-47del NP_002992.1:n.180-47del
NR_103459.1:n.237-47del
NM_001035511.2:c.180-47del NP_001030588.1:n.180-47del
NM_001035512.2:c.78-47del NP_001030589.1:n.78-47del
NM_001035513.2:c.21-47del NP_001030590.1:n.21-47del
NM_001278172.2:c.78-47del NP_001265101.1:n.78-47del
NM_003001.5:c.180-47del MANE Select NP_002992.1:n.180-47del
NR_103459.2:n.232-47del