Canonical Allele Identifier: CA2000554005

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094887G= , CM000673.2:g.112094887G=	GRCh38
NC_000011.9:g.111965611G= , CM000673.1:g.111965611G=	GRCh37
NC_000011.8:g.111470821G=	NCBI36
NG_012337.2:g.13041G=
NG_012337.3:g.13041G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*136G=	ENSP00000432946.2:n.*136G=
ENST00000534010.2:c.314+5876G=	ENSP00000433202.2:n.314+5876G=
ENST00000375549.8:c.397G= MANE Select	ENSP00000364699.3:p.Ala133=
ENST00000528021.6:c.314+5876G=	ENSP00000432465.1:n.314+5876G=
ENST00000375549.7:c.397G=	ENSP00000364699.3:p.Ala133=
ENST00000525291.5:c.280G=	ENSP00000436669.1:p.Ala94=
ENST00000525987.5:n.319+5876G=
ENST00000526592.5:c.*95G=	ENSP00000432005.1:n.*95G=
ENST00000528021.5:c.314+5876G=	ENSP00000432465.1:n.314+5876G=
ENST00000528048.5:c.252G=	ENSP00000436217.1:p.Gln84=
ENST00000528182.5:c.390G=	ENSP00000435475.1:p.Gln130=
ENST00000530923.5:c.441G=
ENST00000531744.5:c.314+5876G=	ENSP00000456957.1:n.314+5876G=
ENST00000532699.1:c.314+5876G=	ENSP00000456434.1:n.314+5876G=
ENST00000534010.1:c.145+5876G=
NM_001276503.1:c.252G=	NP_001263432.1:p.Gln84=
NM_001276504.1:c.280G=	NP_001263433.1:p.Ala94=
NM_001276506.1:c.*95G=	NP_001263435.1:n.*95G=
NM_003002.3:c.397G=	NP_002993.1:p.Ala133=
NR_077060.1:n.535G=
NM_003002.4:c.397G= MANE Select	NP_002993.1:p.Ala133=
NM_001276503.2:c.252G=	NP_001263432.1:p.Gln84=
NM_001276504.2:c.280G=	NP_001263433.1:p.Ala94=
NM_001276506.2:c.*95G=	NP_001263435.1:n.*95G=
NR_077060.2:n.486G=