Canonical Allele Identifier: CA2000554178

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094954T= , CM000673.2:g.112094954T=	GRCh38
NC_000011.9:g.111965678T= , CM000673.1:g.111965678T=	GRCh37
NC_000011.8:g.111470888T=	NCBI36
NG_012337.2:g.13108T=
NG_012337.3:g.13108T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*203T=	ENSP00000432946.2:n.*203T=
ENST00000534010.2:c.314+5943T=	ENSP00000433202.2:n.314+5943T=
ENST00000375549.8:c.464T= MANE Select	ENSP00000364699.3:p.Met155=
ENST00000528021.6:c.314+5943T=	ENSP00000432465.1:n.314+5943T=
ENST00000375549.7:c.464T=	ENSP00000364699.3:p.Met155=
ENST00000525291.5:c.347T=	ENSP00000436669.1:p.Met116=
ENST00000525987.5:n.319+5943T=
ENST00000526592.5:c.*162T=	ENSP00000432005.1:n.*162T=
ENST00000528021.5:c.314+5943T=	ENSP00000432465.1:n.314+5943T=
ENST00000528048.5:c.*61T=	ENSP00000436217.1:n.*61T=
ENST00000528182.5:c.*61T=	ENSP00000435475.1:n.*61T=
ENST00000530923.5:c.508T=
ENST00000531744.5:c.314+5943T=	ENSP00000456957.1:n.314+5943T=
ENST00000532699.1:c.314+5943T=	ENSP00000456434.1:n.314+5943T=
ENST00000534010.1:c.145+5943T=
NM_001276503.1:c.*61T=	NP_001263432.1:n.*61T=
NM_001276504.1:c.347T=	NP_001263433.1:p.Met116=
NM_001276506.1:c.*162T=	NP_001263435.1:n.*162T=
NM_003002.3:c.464T=	NP_002993.1:p.Met155=
NR_077060.1:n.602T=
NM_003002.4:c.464T= MANE Select	NP_002993.1:p.Met155=
NM_001276503.2:c.*61T=	NP_001263432.1:n.*61T=
NM_001276504.2:c.347T=	NP_001263433.1:p.Met116=
NM_001276506.2:c.*162T=	NP_001263435.1:n.*162T=
NR_077060.2:n.553T=