Canonical Allele Identifier: CA421408544

Gene: SDHC

Linked Data

• MyVariant Identifiers: chr1:g.161298258T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328468T>C , CM000663.2:g.161328468T>C	GRCh38
NC_000001.10:g.161298258T>C , CM000663.1:g.161298258T>C	GRCh37
NC_000001.9:g.159564882T>C	NCBI36
NG_012767.1:g.19093T>C , LRG_317:g.19093T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*151T>C	ENSP00000482902.2:n.*151T>C
ENST00000367975.7:c.150T>C MANE Select	ENSP00000356953.3:p.Arg50=
ENST00000342751.8:c.150T>C	ENSP00000356952.3:p.Arg50=
ENST00000367975.6:c.150T>C	ENSP00000356953.2:p.Arg50=
ENST00000392169.6:c.21-12126T>C	ENSP00000376009.2:n.21-12126T>C
ENST00000432287.6:c.77+4798T>C	ENSP00000390558.2:n.77+4798T>C
ENST00000470743.4:c.248T>C
ENST00000504963.5:c.150T>C	ENSP00000423929.1:p.Arg50=
ENST00000513009.5:c.77+4798T>C	ENSP00000423260.1:n.77+4798T>C
ENST00000515731.1:n.624T>C
NM_001035511.1:c.150T>C	NP_001030588.1:p.Arg50=
NM_001035512.1:c.77+4798T>C	NP_001030589.1:n.77+4798T>C
NM_001035513.1:c.21-12126T>C	NP_001030590.1:n.21-12126T>C
NM_001278172.1:c.77+4798T>C	NP_001265101.1:n.77+4798T>C
NM_003001.3:c.150T>C , LRG_317t1:c.150T>C	NP_002992.1:p.Arg50=
NR_103459.1:n.180T>C
NM_001035511.2:c.150T>C	NP_001030588.1:p.Arg50=
NM_001035512.2:c.77+4798T>C	NP_001030589.1:n.77+4798T>C
NM_001035513.2:c.21-12126T>C	NP_001030590.1:n.21-12126T>C
NM_001278172.2:c.77+4798T>C	NP_001265101.1:n.77+4798T>C
NM_003001.5:c.150T>C MANE Select	NP_002992.1:p.Arg50=
NR_103459.2:n.175T>C