Canonical Allele Identifier: CA2000554324

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095141A= , CM000673.2:g.112095141A=	GRCh38
NC_000011.9:g.111965865A= , CM000673.1:g.111965865A=	GRCh37
NC_000011.8:g.111471075A=	NCBI36
NG_012337.2:g.13295A=
NG_012337.3:g.13295A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*390A=	ENSP00000432946.2:n.*390A=
ENST00000534010.2:c.314+6130A=	ENSP00000433202.2:n.314+6130A=
ENST00000375549.8:c.*171A= MANE Select	ENSP00000364699.3:n.*171A=
ENST00000528021.6:c.314+6130A=	ENSP00000432465.1:n.314+6130A=
ENST00000375549.7:c.*171A=	ENSP00000364699.3:n.*171A=
ENST00000525291.5:c.*171A=	ENSP00000436669.1:n.*171A=
ENST00000525987.5:n.319+6130A=
ENST00000526592.5:c.*349A=	ENSP00000432005.1:n.*349A=
ENST00000528021.5:c.314+6130A=	ENSP00000432465.1:n.314+6130A=
ENST00000528048.5:c.*248A=	ENSP00000436217.1:n.*248A=
ENST00000528182.5:c.*248A=	ENSP00000435475.1:n.*248A=
ENST00000530923.5:c.695A=
ENST00000531744.5:c.314+6130A=	ENSP00000456957.1:n.314+6130A=
ENST00000532699.1:c.314+6130A=	ENSP00000456434.1:n.314+6130A=
ENST00000534010.1:c.145+6130A=
NM_001276503.1:c.*248A=	NP_001263432.1:n.*248A=
NM_001276504.1:c.*171A=	NP_001263433.1:n.*171A=
NM_001276506.1:c.*349A=	NP_001263435.1:n.*349A=
NM_003002.3:c.*171A=	NP_002993.1:n.*171A=
NR_077060.1:n.789A=
NM_003002.4:c.*171A= MANE Select	NP_002993.1:n.*171A=
NM_001276503.2:c.*248A=	NP_001263432.1:n.*248A=
NM_001276504.2:c.*171A=	NP_001263433.1:n.*171A=
NM_001276506.2:c.*349A=	NP_001263435.1:n.*349A=
NR_077060.2:n.740A=