Canonical Allele Identifier: CA1148235893
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161314417G= , CM000663.2:g.161314417G= GRCh38
NC_000001.10:g.161284207G= , CM000663.1:g.161284207G= GRCh37
NC_000001.9:g.159550831G= NCBI36
NG_008055.1:g.556C= , LRG_256:g.556C=
NG_012767.1:g.5042G= , LRG_317:g.5042G=

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.12G= ENSP00000482902.2:p.Leu4=
ENST00000367975.7:c.12G= MANE Select ENSP00000356953.3:p.Leu4=
ENST00000342751.8:c.12G= ENSP00000356952.3:p.Leu4=
ENST00000367975.6:c.12G= ENSP00000356953.2:p.Leu4=
ENST00000392169.6:c.12G= ENSP00000376009.2:p.Leu4=
ENST00000432287.6:c.12G= ENSP00000390558.2:p.Leu4=
ENST00000504963.5:c.12G= ENSP00000423929.1:p.Leu4=
ENST00000513009.5:c.12G= ENSP00000423260.1:p.Leu4=
ENST00000515731.1:n.37G=
NM_001035511.1:c.12G= NP_001030588.1:p.Leu4=
NM_001035512.1:c.12G= NP_001030589.1:p.Leu4=
NM_001035513.1:c.12G= NP_001030590.1:p.Leu4=
NM_001278172.1:c.12G= NP_001265101.1:p.Leu4=
NM_003001.3:c.12G= , LRG_317t1:c.12G= NP_002992.1:p.Leu4=
NR_103459.1:n.42G=
NM_001035511.2:c.12G= NP_001030588.1:p.Leu4=
NM_001035512.2:c.12G= NP_001030589.1:p.Leu4=
NM_001035513.2:c.12G= NP_001030590.1:p.Leu4=
NM_001278172.2:c.12G= NP_001265101.1:p.Leu4=
NM_003001.5:c.12G= MANE Select NP_002992.1:p.Leu4=
NR_103459.2:n.37G=