Canonical Allele Identifier: CA2000559919

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086929A= , CM000673.2:g.112086929A=	GRCh38
NC_000011.9:g.111957653A= , CM000673.1:g.111957653A=	GRCh37
NC_000011.8:g.111462863A=	NCBI36
NG_012337.2:g.5083A=
NG_033145.1:g.4870T=
NG_012337.3:g.5083A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.22A=	ENSP00000432946.2:p.Ser8=
ENST00000534010.2:c.22A=	ENSP00000433202.2:p.Ser8=
ENST00000375549.8:c.22A= MANE Select	ENSP00000364699.3:p.Ser8=
ENST00000528021.6:c.22A=	ENSP00000432465.1:p.Ser8=
ENST00000640554.1:c.22A=	ENSP00000491141.1:p.Ser8=
ENST00000375549.7:c.22A=	ENSP00000364699.3:p.Ser8=
ENST00000525291.5:c.22A=	ENSP00000436669.1:p.Ser8=
ENST00000525987.5:n.27A=
ENST00000526592.5:c.22A=	ENSP00000432005.1:p.Ser8=
ENST00000528021.5:c.22A=	ENSP00000432465.1:p.Ser8=
ENST00000528048.5:c.22A=	ENSP00000436217.1:p.Ser8=
ENST00000528182.5:c.22A=	ENSP00000435475.1:p.Ser8=
ENST00000530923.5:c.12A=
ENST00000531744.5:c.22A=	ENSP00000456957.1:p.Ser8=
ENST00000532699.1:c.22A=	ENSP00000456434.1:p.Ser8=
ENST00000614349.4:c.22A=	ENSP00000480666.1:p.Ser8=
NM_001276503.1:c.22A=	NP_001263432.1:p.Ser8=
NM_001276504.1:c.22A=	NP_001263433.1:p.Ser8=
NM_001276506.1:c.22A=	NP_001263435.1:p.Ser8=
NM_003002.3:c.22A=	NP_002993.1:p.Ser8=
NR_077060.1:n.106A=
NM_003002.4:c.22A= MANE Select	NP_002993.1:p.Ser8=
NM_001276503.2:c.22A=	NP_001263432.1:p.Ser8=
NM_001276504.2:c.22A=	NP_001263433.1:p.Ser8=
NM_001276506.2:c.22A=	NP_001263435.1:p.Ser8=
NR_077060.2:n.57A=