Canonical Allele Identifier: CA1202696304

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328445A= , CM000663.2:g.161328445A=	GRCh38
NC_000001.10:g.161298235A= , CM000663.1:g.161298235A=	GRCh37
NC_000001.9:g.159564859A=	NCBI36
NG_012767.1:g.19070A= , LRG_317:g.19070A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*128A=	ENSP00000482902.2:n.*128A=
ENST00000367975.7:c.127A= MANE Select	ENSP00000356953.3:p.Asn43=
ENST00000342751.8:c.127A=	ENSP00000356952.3:p.Asn43=
ENST00000367975.6:c.127A=	ENSP00000356953.2:p.Asn43=
ENST00000392169.6:c.21-12149A=	ENSP00000376009.2:n.21-12149A=
ENST00000432287.6:c.77+4775A=	ENSP00000390558.2:n.77+4775A=
ENST00000470743.4:c.225A=
ENST00000504963.5:c.127A=	ENSP00000423929.1:p.Asn43=
ENST00000513009.5:c.77+4775A=	ENSP00000423260.1:n.77+4775A=
ENST00000515731.1:n.601A=
NM_001035511.1:c.127A=	NP_001030588.1:p.Asn43=
NM_001035512.1:c.77+4775A=	NP_001030589.1:n.77+4775A=
NM_001035513.1:c.21-12149A=	NP_001030590.1:n.21-12149A=
NM_001278172.1:c.77+4775A=	NP_001265101.1:n.77+4775A=
NM_003001.3:c.127A= , LRG_317t1:c.127A=	NP_002992.1:p.Asn43=
NR_103459.1:n.157A=
NM_001035511.2:c.127A=	NP_001030588.1:p.Asn43=
NM_001035512.2:c.77+4775A=	NP_001030589.1:n.77+4775A=
NM_001035513.2:c.21-12149A=	NP_001030590.1:n.21-12149A=
NM_001278172.2:c.77+4775A=	NP_001265101.1:n.77+4775A=
NM_003001.5:c.127A= MANE Select	NP_002992.1:p.Asn43=
NR_103459.2:n.152A=