Canonical Allele Identifier: CA2000554357

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095208G= , CM000673.2:g.112095208G=	GRCh38
NC_000011.9:g.111965932G= , CM000673.1:g.111965932G=	GRCh37
NC_000011.8:g.111471142G=	NCBI36
NG_012337.2:g.13362G=
NG_012337.3:g.13362G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6197G=	ENSP00000433202.2:n.314+6197G=
ENST00000375549.8:c.*238G= MANE Select	ENSP00000364699.3:n.*238G=
ENST00000528021.6:c.314+6197G=	ENSP00000432465.1:n.314+6197G=
ENST00000375549.7:c.*238G=	ENSP00000364699.3:n.*238G=
ENST00000525291.5:c.*238G=	ENSP00000436669.1:n.*238G=
ENST00000525987.5:n.319+6197G=
ENST00000526592.5:c.*416G=	ENSP00000432005.1:n.*416G=
ENST00000528021.5:c.314+6197G=	ENSP00000432465.1:n.314+6197G=
ENST00000528048.5:c.*315G=	ENSP00000436217.1:n.*315G=
ENST00000528182.5:c.*315G=	ENSP00000435475.1:n.*315G=
ENST00000531744.5:c.314+6197G=	ENSP00000456957.1:n.314+6197G=
ENST00000532699.1:c.314+6197G=	ENSP00000456434.1:n.314+6197G=
ENST00000534010.1:c.145+6197G=
NM_001276503.1:c.*315G=	NP_001263432.1:n.*315G=
NM_001276504.1:c.*238G=	NP_001263433.1:n.*238G=
NM_001276506.1:c.*416G=	NP_001263435.1:n.*416G=
NM_003002.3:c.*238G=	NP_002993.1:n.*238G=
NR_077060.1:n.856G=
NM_003002.4:c.*238G= MANE Select	NP_002993.1:n.*238G=
NM_001276503.2:c.*315G=	NP_001263432.1:n.*315G=
NM_001276504.2:c.*238G=	NP_001263433.1:n.*238G=
NM_001276506.2:c.*416G=	NP_001263435.1:n.*416G=
NR_077060.2:n.807G=