Canonical Allele Identifier: CA1202708179
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161356812A= , CM000663.2:g.161356812A= GRCh38
NC_000001.10:g.161326602A= , CM000663.1:g.161326602A= GRCh37
NC_000001.9:g.159593226A= NCBI36
NG_012767.1:g.47437A= , LRG_317:g.47437A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.*378A= ENSP00000482902.2:n.*378A=
ENST00000367975.7:c.377A= MANE Select ENSP00000356953.3:p.Tyr126=
ENST00000342751.8:c.242-5517A= ENSP00000356952.3:n.242-5517A=
ENST00000367975.6:c.377A= ENSP00000356953.2:p.Tyr126=
ENST00000392169.6:c.218A= ENSP00000376009.2:p.Tyr73=
ENST00000432287.6:c.275A= ENSP00000390558.2:p.Tyr92=
ENST00000470743.4:c.475A=
ENST00000504963.5:c.*200A= ENSP00000423929.1:n.*200A=
ENST00000513009.5:c.140-5517A= ENSP00000423260.1:n.140-5517A=
NM_001035511.1:c.242-5517A= NP_001030588.1:n.242-5517A=
NM_001035512.1:c.275A= NP_001030589.1:p.Tyr92=
NM_001035513.1:c.218A= NP_001030590.1:p.Tyr73=
NM_001278172.1:c.140-5517A= NP_001265101.1:n.140-5517A=
NM_003001.3:c.377A= , LRG_317t1:c.377A= NP_002992.1:p.Tyr126=
NR_103459.1:n.434A=
NM_001035511.2:c.242-5517A= NP_001030588.1:n.242-5517A=
NM_001035512.2:c.275A= NP_001030589.1:p.Tyr92=
NM_001035513.2:c.218A= NP_001030590.1:p.Tyr73=
NM_001278172.2:c.140-5517A= NP_001265101.1:n.140-5517A=
NM_003001.5:c.377A= MANE Select NP_002992.1:p.Tyr126=
NR_103459.2:n.429A=