Canonical Allele Identifier: CA382617402

Gene: SDHD

Linked Data

• ClinVar Variation Id: 486440
• ClinVar RCV Id: RCV000563302 ; RCV002526917
• dbSNP Id: rs1555187065
• MyVariant Identifiers: chr11:g.111959719A>G (hg19) ; chr11:g.112088995A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.298A>G	ENSP00000432946.2:p.Thr100Ala
ENST00000534010.2:c.298A>G	ENSP00000433202.2:p.Thr100Ala
ENST00000375549.8:c.298A>G MANE Select	ENSP00000364699.3:p.Thr100Ala
ENST00000528021.6:c.298A>G	ENSP00000432465.1:p.Thr100Ala
ENST00000640554.1:c.*370A>G	ENSP00000491141.1:n.*370A>G
ENST00000375549.7:c.298A>G	ENSP00000364699.3:p.Thr100Ala
ENST00000525291.5:c.181A>G	ENSP00000436669.1:p.Thr61Ala
ENST00000525987.5:n.303A>G
ENST00000526592.5:c.298A>G	ENSP00000432005.1:p.Thr100Ala
ENST00000528021.5:c.298A>G	ENSP00000432465.1:p.Thr100Ala
ENST00000528048.5:c.169+1022A>G	ENSP00000436217.1:n.169+1022A>G
ENST00000528182.5:c.298A>G	ENSP00000435475.1:p.Thr100Ala
ENST00000530923.5:c.288A>G
ENST00000531744.5:c.298A>G	ENSP00000456957.1:p.Thr100Ala
ENST00000532699.1:c.298A>G	ENSP00000456434.1:p.Thr100Ala
ENST00000534010.1:c.129A>G
ENST00000614349.4:c.298A>G	ENSP00000480666.1:p.Thr100Ala
NM_001276503.1:c.169+1022A>G	NP_001263432.1:n.169+1022A>G
NM_001276504.1:c.181A>G	NP_001263433.1:p.Thr61Ala
NM_001276506.1:c.298A>G	NP_001263435.1:p.Thr100Ala
NM_003002.3:c.298A>G	NP_002993.1:p.Thr100Ala
NR_077060.1:n.382A>G
NM_003002.4:c.298A>G MANE Select	NP_002993.1:p.Thr100Ala
NM_001276503.2:c.169+1022A>G	NP_001263432.1:n.169+1022A>G
NM_001276504.2:c.181A>G	NP_001263433.1:p.Thr61Ala
NM_001276506.2:c.298A>G	NP_001263435.1:p.Thr100Ala
NR_077060.2:n.333A>G