Canonical Allele Identifier: CA2000554113

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094933G= , CM000673.2:g.112094933G=	GRCh38
NC_000011.9:g.111965657G= , CM000673.1:g.111965657G=	GRCh37
NC_000011.8:g.111470867G=	NCBI36
NG_012337.2:g.13087G=
NG_012337.3:g.13087G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*182G=	ENSP00000432946.2:n.*182G=
ENST00000534010.2:c.314+5922G=	ENSP00000433202.2:n.314+5922G=
ENST00000375549.8:c.443G= MANE Select	ENSP00000364699.3:p.Gly148=
ENST00000528021.6:c.314+5922G=	ENSP00000432465.1:n.314+5922G=
ENST00000375549.7:c.443G=	ENSP00000364699.3:p.Gly148=
ENST00000525291.5:c.326G=	ENSP00000436669.1:p.Gly109=
ENST00000525987.5:n.319+5922G=
ENST00000526592.5:c.*141G=	ENSP00000432005.1:n.*141G=
ENST00000528021.5:c.314+5922G=	ENSP00000432465.1:n.314+5922G=
ENST00000528048.5:c.*40G=	ENSP00000436217.1:n.*40G=
ENST00000528182.5:c.*40G=	ENSP00000435475.1:n.*40G=
ENST00000530923.5:c.487G=
ENST00000531744.5:c.314+5922G=	ENSP00000456957.1:n.314+5922G=
ENST00000532699.1:c.314+5922G=	ENSP00000456434.1:n.314+5922G=
ENST00000534010.1:c.145+5922G=
NM_001276503.1:c.*40G=	NP_001263432.1:n.*40G=
NM_001276504.1:c.326G=	NP_001263433.1:p.Gly109=
NM_001276506.1:c.*141G=	NP_001263435.1:n.*141G=
NM_003002.3:c.443G=	NP_002993.1:p.Gly148=
NR_077060.1:n.581G=
NM_003002.4:c.443G= MANE Select	NP_002993.1:p.Gly148=
NM_001276503.2:c.*40G=	NP_001263432.1:n.*40G=
NM_001276504.2:c.326G=	NP_001263433.1:p.Gly109=
NM_001276506.2:c.*141G=	NP_001263435.1:n.*141G=
NR_077060.2:n.532G=