Canonical Allele Identifier: CA2000554302

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095083C= , CM000673.2:g.112095083C=	GRCh38
NC_000011.9:g.111965807C= , CM000673.1:g.111965807C=	GRCh37
NC_000011.8:g.111471017C=	NCBI36
NG_012337.2:g.13237C=
NG_012337.3:g.13237C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*332C=	ENSP00000432946.2:n.*332C=
ENST00000534010.2:c.314+6072C=	ENSP00000433202.2:n.314+6072C=
ENST00000375549.8:c.*113C= MANE Select	ENSP00000364699.3:n.*113C=
ENST00000528021.6:c.314+6072C=	ENSP00000432465.1:n.314+6072C=
ENST00000375549.7:c.*113C=	ENSP00000364699.3:n.*113C=
ENST00000525291.5:c.*113C=	ENSP00000436669.1:n.*113C=
ENST00000525987.5:n.319+6072C=
ENST00000526592.5:c.*291C=	ENSP00000432005.1:n.*291C=
ENST00000528021.5:c.314+6072C=	ENSP00000432465.1:n.314+6072C=
ENST00000528048.5:c.*190C=	ENSP00000436217.1:n.*190C=
ENST00000528182.5:c.*190C=	ENSP00000435475.1:n.*190C=
ENST00000530923.5:c.637C=
ENST00000531744.5:c.314+6072C=	ENSP00000456957.1:n.314+6072C=
ENST00000532699.1:c.314+6072C=	ENSP00000456434.1:n.314+6072C=
ENST00000534010.1:c.145+6072C=
NM_001276503.1:c.*190C=	NP_001263432.1:n.*190C=
NM_001276504.1:c.*113C=	NP_001263433.1:n.*113C=
NM_001276506.1:c.*291C=	NP_001263435.1:n.*291C=
NM_003002.3:c.*113C=	NP_002993.1:n.*113C=
NR_077060.1:n.731C=
NM_003002.4:c.*113C= MANE Select	NP_002993.1:n.*113C=
NM_001276503.2:c.*190C=	NP_001263432.1:n.*190C=
NM_001276504.2:c.*113C=	NP_001263433.1:n.*113C=
NM_001276506.2:c.*291C=	NP_001263435.1:n.*291C=
NR_077060.2:n.682C=