Canonical Allele Identifier: CA1202708271
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161357033A= , CM000663.2:g.161357033A= GRCh38
NC_000001.10:g.161326823A= , CM000663.1:g.161326823A= GRCh37
NC_000001.9:g.159593447A= NCBI36
NG_012767.1:g.47658A= , LRG_317:g.47658A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*406+193A= ENSP00000482902.2:n.*406+193A=
ENST00000367975.7:c.405+193A= MANE Select ENSP00000356953.3:n.405+193A=
ENST00000342751.8:c.242-5296A= ENSP00000356952.3:n.242-5296A=
ENST00000367975.6:c.405+193A= ENSP00000356953.2:n.405+193A=
ENST00000392169.6:c.246+193A= ENSP00000376009.2:n.246+193A=
ENST00000432287.6:c.303+193A= ENSP00000390558.2:n.303+193A=
ENST00000470743.4:c.503+193A=
ENST00000504963.5:c.*228+193A= ENSP00000423929.1:n.*228+193A=
ENST00000513009.5:c.140-5296A= ENSP00000423260.1:n.140-5296A=
NM_001035511.1:c.242-5296A= NP_001030588.1:n.242-5296A=
NM_001035512.1:c.303+193A= NP_001030589.1:n.303+193A=
NM_001035513.1:c.246+193A= NP_001030590.1:n.246+193A=
NM_001278172.1:c.140-5296A= NP_001265101.1:n.140-5296A=
NM_003001.3:c.405+193A= , LRG_317t1:c.405+193A= NP_002992.1:n.405+193A=
NR_103459.1:n.462+193A=
NM_001035511.2:c.242-5296A= NP_001030588.1:n.242-5296A=
NM_001035512.2:c.303+193A= NP_001030589.1:n.303+193A=
NM_001035513.2:c.246+193A= NP_001030590.1:n.246+193A=
NM_001278172.2:c.140-5296A= NP_001265101.1:n.140-5296A=
NM_003001.5:c.405+193A= MANE Select NP_002992.1:n.405+193A=
NR_103459.2:n.457+193A=