Canonical Allele Identifier: CA2000554417

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095282G= , CM000673.2:g.112095282G=	GRCh38
NC_000011.9:g.111966006G= , CM000673.1:g.111966006G=	GRCh37
NC_000011.8:g.111471216G=	NCBI36
NG_012337.2:g.13436G=
NG_012337.3:g.13436G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6271G=	ENSP00000433202.2:n.314+6271G=
ENST00000375549.8:c.*312G= MANE Select	ENSP00000364699.3:n.*312G=
ENST00000528021.6:c.314+6271G=	ENSP00000432465.1:n.314+6271G=
ENST00000375549.7:c.*312G=	ENSP00000364699.3:n.*312G=
ENST00000525291.5:c.*312G=	ENSP00000436669.1:n.*312G=
ENST00000525987.5:n.319+6271G=
ENST00000528021.5:c.314+6271G=	ENSP00000432465.1:n.314+6271G=
ENST00000528048.5:c.*389G=	ENSP00000436217.1:n.*389G=
ENST00000531744.5:c.314+6271G=	ENSP00000456957.1:n.314+6271G=
ENST00000532699.1:c.314+6271G=	ENSP00000456434.1:n.314+6271G=
ENST00000534010.1:c.145+6271G=
NM_001276503.1:c.*389G=	NP_001263432.1:n.*389G=
NM_001276504.1:c.*312G=	NP_001263433.1:n.*312G=
NM_001276506.1:c.*490G=	NP_001263435.1:n.*490G=
NM_003002.3:c.*312G=	NP_002993.1:n.*312G=
NR_077060.1:n.930G=
NM_003002.4:c.*312G= MANE Select	NP_002993.1:n.*312G=
NM_001276503.2:c.*389G=	NP_001263432.1:n.*389G=
NM_001276504.2:c.*312G=	NP_001263433.1:n.*312G=
NM_001276506.2:c.*490G=	NP_001263435.1:n.*490G=
NR_077060.2:n.881G=