Canonical Allele Identifier: CA2000554236

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094997T= , CM000673.2:g.112094997T=	GRCh38
NC_000011.9:g.111965721T= , CM000673.1:g.111965721T=	GRCh37
NC_000011.8:g.111470931T=	NCBI36
NG_012337.2:g.13151T=
NG_012337.3:g.13151T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*246T=	ENSP00000432946.2:n.*246T=
ENST00000534010.2:c.314+5986T=	ENSP00000433202.2:n.314+5986T=
ENST00000375549.8:c.*27T= MANE Select	ENSP00000364699.3:n.*27T=
ENST00000528021.6:c.314+5986T=	ENSP00000432465.1:n.314+5986T=
ENST00000375549.7:c.*27T=	ENSP00000364699.3:n.*27T=
ENST00000525291.5:c.*27T=	ENSP00000436669.1:n.*27T=
ENST00000525987.5:n.319+5986T=
ENST00000526592.5:c.*205T=	ENSP00000432005.1:n.*205T=
ENST00000528021.5:c.314+5986T=	ENSP00000432465.1:n.314+5986T=
ENST00000528048.5:c.*104T=	ENSP00000436217.1:n.*104T=
ENST00000528182.5:c.*104T=	ENSP00000435475.1:n.*104T=
ENST00000530923.5:c.551T=
ENST00000531744.5:c.314+5986T=	ENSP00000456957.1:n.314+5986T=
ENST00000532699.1:c.314+5986T=	ENSP00000456434.1:n.314+5986T=
ENST00000534010.1:c.145+5986T=
NM_001276503.1:c.*104T=	NP_001263432.1:n.*104T=
NM_001276504.1:c.*27T=	NP_001263433.1:n.*27T=
NM_001276506.1:c.*205T=	NP_001263435.1:n.*205T=
NM_003002.3:c.*27T=	NP_002993.1:n.*27T=
NR_077060.1:n.645T=
NM_003002.4:c.*27T= MANE Select	NP_002993.1:n.*27T=
NM_001276503.2:c.*104T=	NP_001263432.1:n.*104T=
NM_001276504.2:c.*27T=	NP_001263433.1:n.*27T=
NM_001276506.2:c.*205T=	NP_001263435.1:n.*205T=
NR_077060.2:n.596T=