Canonical Allele Identifier: CA1140024216

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161362850G= , CM000663.2:g.161362850G=	GRCh38
NC_000001.10:g.161332640G= , CM000663.1:g.161332640G=	GRCh37
NC_000001.9:g.159599264G=	NCBI36
NG_012767.1:g.53475G= , LRG_317:g.53475G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*928G=	ENSP00000482902.2:n.*928G=
ENST00000367975.7:c.*417G= MANE Select	ENSP00000356953.3:n.*417G=
ENST00000342751.8:c.*310G=	ENSP00000356952.3:n.*310G=
ENST00000367975.6:c.*417G=	ENSP00000356953.2:n.*417G=
NM_001035511.1:c.*310G=	NP_001030588.1:n.*310G=
NM_001035512.1:c.*417G=	NP_001030589.1:n.*417G=
NM_001035513.1:c.*417G=	NP_001030590.1:n.*417G=
NM_001278172.1:c.*310G=	NP_001265101.1:n.*310G=
NM_003001.3:c.*417G= , LRG_317t1:c.*417G=	NP_002992.1:n.*417G=
NR_103459.1:n.984G=
NM_001035511.2:c.*310G=	NP_001030588.1:n.*310G=
NM_001035512.2:c.*417G=	NP_001030589.1:n.*417G=
NM_001035513.2:c.*417G=	NP_001030590.1:n.*417G=
NM_001278172.2:c.*310G=	NP_001265101.1:n.*310G=
NM_003001.5:c.*417G= MANE Select	NP_002992.1:n.*417G=
NR_103459.2:n.979G=