Canonical Allele Identifier: CA2000554412

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095276C= , CM000673.2:g.112095276C=	GRCh38
NC_000011.9:g.111966000C= , CM000673.1:g.111966000C=	GRCh37
NC_000011.8:g.111471210C=	NCBI36
NG_012337.2:g.13430C=
NG_012337.3:g.13430C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6265C=	ENSP00000433202.2:n.314+6265C=
ENST00000375549.8:c.*306C= MANE Select	ENSP00000364699.3:n.*306C=
ENST00000528021.6:c.314+6265C=	ENSP00000432465.1:n.314+6265C=
ENST00000375549.7:c.*306C=	ENSP00000364699.3:n.*306C=
ENST00000525291.5:c.*306C=	ENSP00000436669.1:n.*306C=
ENST00000525987.5:n.319+6265C=
ENST00000528021.5:c.314+6265C=	ENSP00000432465.1:n.314+6265C=
ENST00000528048.5:c.*383C=	ENSP00000436217.1:n.*383C=
ENST00000531744.5:c.314+6265C=	ENSP00000456957.1:n.314+6265C=
ENST00000532699.1:c.314+6265C=	ENSP00000456434.1:n.314+6265C=
ENST00000534010.1:c.145+6265C=
NM_001276503.1:c.*383C=	NP_001263432.1:n.*383C=
NM_001276504.1:c.*306C=	NP_001263433.1:n.*306C=
NM_001276506.1:c.*484C=	NP_001263435.1:n.*484C=
NM_003002.3:c.*306C=	NP_002993.1:n.*306C=
NR_077060.1:n.924C=
NM_003002.4:c.*306C= MANE Select	NP_002993.1:n.*306C=
NM_001276503.2:c.*383C=	NP_001263432.1:n.*383C=
NM_001276504.2:c.*306C=	NP_001263433.1:n.*306C=
NM_001276506.2:c.*484C=	NP_001263435.1:n.*484C=
NR_077060.2:n.875C=