Canonical Allele Identifier: CA2000561869

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088874C= , CM000673.2:g.112088874C=	GRCh38
NC_000011.9:g.111959598C= , CM000673.1:g.111959598C=	GRCh37
NC_000011.8:g.111464808C=	NCBI36
NG_012337.2:g.7028C=
NG_033145.1:g.2925G=
NG_012337.3:g.7028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.177C=	ENSP00000432946.2:p.Ser59=
ENST00000534010.2:c.177C=	ENSP00000433202.2:p.Ser59=
ENST00000375549.8:c.177C= MANE Select	ENSP00000364699.3:p.Ser59=
ENST00000528021.6:c.177C=	ENSP00000432465.1:p.Ser59=
ENST00000640554.1:c.*249C=	ENSP00000491141.1:n.*249C=
ENST00000375549.7:c.177C=	ENSP00000364699.3:p.Ser59=
ENST00000525291.5:c.60C=	ENSP00000436669.1:p.Ser20=
ENST00000525987.5:n.182C=
ENST00000526592.5:c.177C=	ENSP00000432005.1:p.Ser59=
ENST00000528021.5:c.177C=	ENSP00000432465.1:p.Ser59=
ENST00000528048.5:c.169+901C=	ENSP00000436217.1:n.169+901C=
ENST00000528182.5:c.177C=	ENSP00000435475.1:p.Ser59=
ENST00000530923.5:c.167C=
ENST00000531744.5:c.177C=	ENSP00000456957.1:p.Ser59=
ENST00000532699.1:c.177C=	ENSP00000456434.1:p.Ser59=
ENST00000534010.1:c.8C=
ENST00000614349.4:c.177C=	ENSP00000480666.1:p.Ser59=
NM_001276503.1:c.169+901C=	NP_001263432.1:n.169+901C=
NM_001276504.1:c.60C=	NP_001263433.1:p.Ser20=
NM_001276506.1:c.177C=	NP_001263435.1:p.Ser59=
NM_003002.3:c.177C=	NP_002993.1:p.Ser59=
NR_077060.1:n.261C=
NM_003002.4:c.177C= MANE Select	NP_002993.1:p.Ser59=
NM_001276503.2:c.169+901C=	NP_001263432.1:n.169+901C=
NM_001276504.2:c.60C=	NP_001263433.1:p.Ser20=
NM_001276506.2:c.177C=	NP_001263435.1:p.Ser59=
NR_077060.2:n.212C=