Canonical Allele Identifier: CA1202696360

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328478C= , CM000663.2:g.161328478C=	GRCh38
NC_000001.10:g.161298268C= , CM000663.1:g.161298268C=	GRCh37
NC_000001.9:g.159564892C=	NCBI36
NG_012767.1:g.19103C= , LRG_317:g.19103C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*161C=	ENSP00000482902.2:n.*161C=
ENST00000367975.7:c.160C= MANE Select	ENSP00000356953.3:p.Pro54=
ENST00000342751.8:c.160C=	ENSP00000356952.3:p.Pro54=
ENST00000367975.6:c.160C=	ENSP00000356953.2:p.Pro54=
ENST00000392169.6:c.21-12116C=	ENSP00000376009.2:n.21-12116C=
ENST00000432287.6:c.77+4808C=	ENSP00000390558.2:n.77+4808C=
ENST00000470743.4:c.258C=
ENST00000504963.5:c.160C=	ENSP00000423929.1:p.Pro54=
ENST00000513009.5:c.77+4808C=	ENSP00000423260.1:n.77+4808C=
ENST00000515731.1:n.634C=
NM_001035511.1:c.160C=	NP_001030588.1:p.Pro54=
NM_001035512.1:c.77+4808C=	NP_001030589.1:n.77+4808C=
NM_001035513.1:c.21-12116C=	NP_001030590.1:n.21-12116C=
NM_001278172.1:c.77+4808C=	NP_001265101.1:n.77+4808C=
NM_003001.3:c.160C= , LRG_317t1:c.160C=	NP_002992.1:p.Pro54=
NR_103459.1:n.190C=
NM_001035511.2:c.160C=	NP_001030588.1:p.Pro54=
NM_001035512.2:c.77+4808C=	NP_001030589.1:n.77+4808C=
NM_001035513.2:c.21-12116C=	NP_001030590.1:n.21-12116C=
NM_001278172.2:c.77+4808C=	NP_001265101.1:n.77+4808C=
NM_003001.5:c.160C= MANE Select	NP_002992.1:p.Pro54=
NR_103459.2:n.185C=