Canonical Allele Identifier: CA382618730

Gene: SDHD

Linked Data

• ClinVar Variation Id: 480806
• ClinVar RCV Id: RCV000561906 ; RCV000660262 ; RCV002232089 ; RCV003420005
• dbSNP Id: rs1555187574
• MyVariant Identifiers: chr11:g.111965531G>T (hg19) ; chr11:g.112094807G>T (hg38)
• PubMed: PMID:19351833

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094807G>T , CM000673.2:g.112094807G>T	GRCh38
NC_000011.9:g.111965531G>T , CM000673.1:g.111965531G>T	GRCh37
NC_000011.8:g.111470741G>T	NCBI36
NG_012337.2:g.12961G>T
NG_012337.3:g.12961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*56G>T	ENSP00000432946.2:n.*56G>T
ENST00000534010.2:c.314+5796G>T	ENSP00000433202.2:n.314+5796G>T
ENST00000375549.8:c.317G>T MANE Select	ENSP00000364699.3:p.Gly106Val
ENST00000528021.6:c.314+5796G>T	ENSP00000432465.1:n.314+5796G>T
ENST00000375549.7:c.317G>T	ENSP00000364699.3:p.Gly106Val
ENST00000525291.5:c.200G>T	ENSP00000436669.1:p.Gly67Val
ENST00000525987.5:n.319+5796G>T
ENST00000526592.5:c.*15G>T	ENSP00000432005.1:n.*15G>T
ENST00000528021.5:c.314+5796G>T	ENSP00000432465.1:n.314+5796G>T
ENST00000528048.5:c.172G>T	ENSP00000436217.1:p.Ala58Ser
ENST00000528182.5:c.310G>T	ENSP00000435475.1:p.Ala104Ser
ENST00000530923.5:c.361G>T
ENST00000531744.5:c.314+5796G>T	ENSP00000456957.1:n.314+5796G>T
ENST00000532699.1:c.314+5796G>T	ENSP00000456434.1:n.314+5796G>T
ENST00000534010.1:c.145+5796G>T
NM_001276503.1:c.172G>T	NP_001263432.1:p.Ala58Ser
NM_001276504.1:c.200G>T	NP_001263433.1:p.Gly67Val
NM_001276506.1:c.*15G>T	NP_001263435.1:n.*15G>T
NM_003002.3:c.317G>T	NP_002993.1:p.Gly106Val
NR_077060.1:n.455G>T
NM_003002.4:c.317G>T MANE Select	NP_002993.1:p.Gly106Val
NM_001276503.2:c.172G>T	NP_001263432.1:p.Ala58Ser
NM_001276504.2:c.200G>T	NP_001263433.1:p.Gly67Val
NM_001276506.2:c.*15G>T	NP_001263435.1:n.*15G>T
NR_077060.2:n.406G>T