Canonical Allele Identifier: CA2000554315

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095117T= , CM000673.2:g.112095117T=	GRCh38
NC_000011.9:g.111965841T= , CM000673.1:g.111965841T=	GRCh37
NC_000011.8:g.111471051T=	NCBI36
NG_012337.2:g.13271T=
NG_012337.3:g.13271T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*366T=	ENSP00000432946.2:n.*366T=
ENST00000534010.2:c.314+6106T=	ENSP00000433202.2:n.314+6106T=
ENST00000375549.8:c.*147T= MANE Select	ENSP00000364699.3:n.*147T=
ENST00000528021.6:c.314+6106T=	ENSP00000432465.1:n.314+6106T=
ENST00000375549.7:c.*147T=	ENSP00000364699.3:n.*147T=
ENST00000525291.5:c.*147T=	ENSP00000436669.1:n.*147T=
ENST00000525987.5:n.319+6106T=
ENST00000526592.5:c.*325T=	ENSP00000432005.1:n.*325T=
ENST00000528021.5:c.314+6106T=	ENSP00000432465.1:n.314+6106T=
ENST00000528048.5:c.*224T=	ENSP00000436217.1:n.*224T=
ENST00000528182.5:c.*224T=	ENSP00000435475.1:n.*224T=
ENST00000530923.5:c.671T=
ENST00000531744.5:c.314+6106T=	ENSP00000456957.1:n.314+6106T=
ENST00000532699.1:c.314+6106T=	ENSP00000456434.1:n.314+6106T=
ENST00000534010.1:c.145+6106T=
NM_001276503.1:c.*224T=	NP_001263432.1:n.*224T=
NM_001276504.1:c.*147T=	NP_001263433.1:n.*147T=
NM_001276506.1:c.*325T=	NP_001263435.1:n.*325T=
NM_003002.3:c.*147T=	NP_002993.1:n.*147T=
NR_077060.1:n.765T=
NM_003002.4:c.*147T= MANE Select	NP_002993.1:n.*147T=
NM_001276503.2:c.*224T=	NP_001263432.1:n.*224T=
NM_001276504.2:c.*147T=	NP_001263433.1:n.*147T=
NM_001276506.2:c.*325T=	NP_001263435.1:n.*325T=
NR_077060.2:n.716T=