Canonical Allele Identifier: CA2000562145

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088995A= , CM000673.2:g.112088995A=	GRCh38
NC_000011.9:g.111959719A= , CM000673.1:g.111959719A=	GRCh37
NC_000011.8:g.111464929A=	NCBI36
NG_012337.2:g.7149A=
NG_033145.1:g.2804T=
NG_012337.3:g.7149A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.298A=	ENSP00000432946.2:p.Thr100=
ENST00000534010.2:c.298A=	ENSP00000433202.2:p.Thr100=
ENST00000375549.8:c.298A= MANE Select	ENSP00000364699.3:p.Thr100=
ENST00000528021.6:c.298A=	ENSP00000432465.1:p.Thr100=
ENST00000640554.1:c.*370A=	ENSP00000491141.1:n.*370A=
ENST00000375549.7:c.298A=	ENSP00000364699.3:p.Thr100=
ENST00000525291.5:c.181A=	ENSP00000436669.1:p.Thr61=
ENST00000525987.5:n.303A=
ENST00000526592.5:c.298A=	ENSP00000432005.1:p.Thr100=
ENST00000528021.5:c.298A=	ENSP00000432465.1:p.Thr100=
ENST00000528048.5:c.169+1022A=	ENSP00000436217.1:n.169+1022A=
ENST00000528182.5:c.298A=	ENSP00000435475.1:p.Thr100=
ENST00000530923.5:c.288A=
ENST00000531744.5:c.298A=	ENSP00000456957.1:p.Thr100=
ENST00000532699.1:c.298A=	ENSP00000456434.1:p.Thr100=
ENST00000534010.1:c.129A=
ENST00000614349.4:c.298A=	ENSP00000480666.1:p.Thr100=
NM_001276503.1:c.169+1022A=	NP_001263432.1:n.169+1022A=
NM_001276504.1:c.181A=	NP_001263433.1:p.Thr61=
NM_001276506.1:c.298A=	NP_001263435.1:p.Thr100=
NM_003002.3:c.298A=	NP_002993.1:p.Thr100=
NR_077060.1:n.382A=
NM_003002.4:c.298A= MANE Select	NP_002993.1:p.Thr100=
NM_001276503.2:c.169+1022A=	NP_001263432.1:n.169+1022A=
NM_001276504.2:c.181A=	NP_001263433.1:p.Thr61=
NM_001276506.2:c.298A=	NP_001263435.1:p.Thr100=
NR_077060.2:n.333A=