Canonical Allele Identifier: CA2000554323

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095136G= , CM000673.2:g.112095136G=	GRCh38
NC_000011.9:g.111965860G= , CM000673.1:g.111965860G=	GRCh37
NC_000011.8:g.111471070G=	NCBI36
NG_012337.2:g.13290G=
NG_012337.3:g.13290G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*385G=	ENSP00000432946.2:n.*385G=
ENST00000534010.2:c.314+6125G=	ENSP00000433202.2:n.314+6125G=
ENST00000375549.8:c.*166G= MANE Select	ENSP00000364699.3:n.*166G=
ENST00000528021.6:c.314+6125G=	ENSP00000432465.1:n.314+6125G=
ENST00000375549.7:c.*166G=	ENSP00000364699.3:n.*166G=
ENST00000525291.5:c.*166G=	ENSP00000436669.1:n.*166G=
ENST00000525987.5:n.319+6125G=
ENST00000526592.5:c.*344G=	ENSP00000432005.1:n.*344G=
ENST00000528021.5:c.314+6125G=	ENSP00000432465.1:n.314+6125G=
ENST00000528048.5:c.*243G=	ENSP00000436217.1:n.*243G=
ENST00000528182.5:c.*243G=	ENSP00000435475.1:n.*243G=
ENST00000530923.5:c.690G=
ENST00000531744.5:c.314+6125G=	ENSP00000456957.1:n.314+6125G=
ENST00000532699.1:c.314+6125G=	ENSP00000456434.1:n.314+6125G=
ENST00000534010.1:c.145+6125G=
NM_001276503.1:c.*243G=	NP_001263432.1:n.*243G=
NM_001276504.1:c.*166G=	NP_001263433.1:n.*166G=
NM_001276506.1:c.*344G=	NP_001263435.1:n.*344G=
NM_003002.3:c.*166G=	NP_002993.1:n.*166G=
NR_077060.1:n.784G=
NM_003002.4:c.*166G= MANE Select	NP_002993.1:n.*166G=
NM_001276503.2:c.*243G=	NP_001263432.1:n.*243G=
NM_001276504.2:c.*166G=	NP_001263433.1:n.*166G=
NM_001276506.2:c.*344G=	NP_001263435.1:n.*344G=
NR_077060.2:n.735G=