Canonical Allele Identifier: CA1202701733
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161340448G= , CM000663.2:g.161340448G= GRCh38
NC_000001.10:g.161310238G= , CM000663.1:g.161310238G= GRCh37
NC_000001.9:g.159576862G= NCBI36
NG_012767.1:g.31073G= , LRG_317:g.31073G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*181-146G= ENSP00000482902.2:n.*181-146G=
ENST00000367975.7:c.180-146G= MANE Select ENSP00000356953.3:n.180-146G=
ENST00000342751.8:c.180-146G= ENSP00000356952.3:n.180-146G=
ENST00000367975.6:c.180-146G= ENSP00000356953.2:n.180-146G=
ENST00000392169.6:c.21-146G= ENSP00000376009.2:n.21-146G=
ENST00000432287.6:c.78-146G= ENSP00000390558.2:n.78-146G=
ENST00000470743.4:c.278-146G=
ENST00000504963.5:c.*3-146G= ENSP00000423929.1:n.*3-146G=
ENST00000513009.5:c.78-146G= ENSP00000423260.1:n.78-146G=
NM_001035511.1:c.180-146G= NP_001030588.1:n.180-146G=
NM_001035512.1:c.78-146G= NP_001030589.1:n.78-146G=
NM_001035513.1:c.21-146G= NP_001030590.1:n.21-146G=
NM_001278172.1:c.78-146G= NP_001265101.1:n.78-146G=
NM_003001.3:c.180-146G= , LRG_317t1:c.180-146G= NP_002992.1:n.180-146G=
NR_103459.1:n.237-146G=
NM_001035511.2:c.180-146G= NP_001030588.1:n.180-146G=
NM_001035512.2:c.78-146G= NP_001030589.1:n.78-146G=
NM_001035513.2:c.21-146G= NP_001030590.1:n.21-146G=
NM_001278172.2:c.78-146G= NP_001265101.1:n.78-146G=
NM_003001.5:c.180-146G= MANE Select NP_002992.1:n.180-146G=
NR_103459.2:n.232-146G=