Canonical Allele Identifier: CA2000554318

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095125T= , CM000673.2:g.112095125T=	GRCh38
NC_000011.9:g.111965849T= , CM000673.1:g.111965849T=	GRCh37
NC_000011.8:g.111471059T=	NCBI36
NG_012337.2:g.13279T=
NG_012337.3:g.13279T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*374T=	ENSP00000432946.2:n.*374T=
ENST00000534010.2:c.314+6114T=	ENSP00000433202.2:n.314+6114T=
ENST00000375549.8:c.*155T= MANE Select	ENSP00000364699.3:n.*155T=
ENST00000528021.6:c.314+6114T=	ENSP00000432465.1:n.314+6114T=
ENST00000375549.7:c.*155T=	ENSP00000364699.3:n.*155T=
ENST00000525291.5:c.*155T=	ENSP00000436669.1:n.*155T=
ENST00000525987.5:n.319+6114T=
ENST00000526592.5:c.*333T=	ENSP00000432005.1:n.*333T=
ENST00000528021.5:c.314+6114T=	ENSP00000432465.1:n.314+6114T=
ENST00000528048.5:c.*232T=	ENSP00000436217.1:n.*232T=
ENST00000528182.5:c.*232T=	ENSP00000435475.1:n.*232T=
ENST00000530923.5:c.679T=
ENST00000531744.5:c.314+6114T=	ENSP00000456957.1:n.314+6114T=
ENST00000532699.1:c.314+6114T=	ENSP00000456434.1:n.314+6114T=
ENST00000534010.1:c.145+6114T=
NM_001276503.1:c.*232T=	NP_001263432.1:n.*232T=
NM_001276504.1:c.*155T=	NP_001263433.1:n.*155T=
NM_001276506.1:c.*333T=	NP_001263435.1:n.*333T=
NM_003002.3:c.*155T=	NP_002993.1:n.*155T=
NR_077060.1:n.773T=
NM_003002.4:c.*155T= MANE Select	NP_002993.1:n.*155T=
NM_001276503.2:c.*232T=	NP_001263432.1:n.*232T=
NM_001276504.2:c.*155T=	NP_001263433.1:n.*155T=
NM_001276506.2:c.*333T=	NP_001263435.1:n.*333T=
NR_077060.2:n.724T=