Canonical Allele Identifier: CA071433

Gene: SDHD

Linked Data

• ClinVar Variation Id: 239472
• ClinVar RCV Id: RCV001753697 ; RCV002229351 ; RCV002338724
• dbSNP Id: rs761953172
• ExAC: 11:111965667 A / C
• gnomAD v2: 11-111965667-A-C
• gnomAD v4: 11-112094943-A-C
• MyVariant Identifiers: chr11:g.111965667A>C (hg19) ; chr11:g.112094943A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094943A>C , CM000673.2:g.112094943A>C	GRCh38
NC_000011.9:g.111965667A>C , CM000673.1:g.111965667A>C	GRCh37
NC_000011.8:g.111470877A>C	NCBI36
NG_012337.2:g.13097A>C
NG_012337.3:g.13097A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*192A>C	ENSP00000432946.2:n.*192A>C
ENST00000534010.2:c.314+5932A>C	ENSP00000433202.2:n.314+5932A>C
ENST00000375549.8:c.453A>C MANE Select	ENSP00000364699.3:p.Lys151Asn
ENST00000528021.6:c.314+5932A>C	ENSP00000432465.1:n.314+5932A>C
ENST00000375549.7:c.453A>C	ENSP00000364699.3:p.Lys151Asn
ENST00000525291.5:c.336A>C	ENSP00000436669.1:p.Lys112Asn
ENST00000525987.5:n.319+5932A>C
ENST00000526592.5:c.*151A>C	ENSP00000432005.1:n.*151A>C
ENST00000528021.5:c.314+5932A>C	ENSP00000432465.1:n.314+5932A>C
ENST00000528048.5:c.*50A>C	ENSP00000436217.1:n.*50A>C
ENST00000528182.5:c.*50A>C	ENSP00000435475.1:n.*50A>C
ENST00000530923.5:c.497A>C
ENST00000531744.5:c.314+5932A>C	ENSP00000456957.1:n.314+5932A>C
ENST00000532699.1:c.314+5932A>C	ENSP00000456434.1:n.314+5932A>C
ENST00000534010.1:c.145+5932A>C
NM_001276503.1:c.*50A>C	NP_001263432.1:n.*50A>C
NM_001276504.1:c.336A>C	NP_001263433.1:p.Lys112Asn
NM_001276506.1:c.*151A>C	NP_001263435.1:n.*151A>C
NM_003002.3:c.453A>C	NP_002993.1:p.Lys151Asn
NR_077060.1:n.591A>C
NM_003002.4:c.453A>C MANE Select	NP_002993.1:p.Lys151Asn
NM_001276503.2:c.*50A>C	NP_001263432.1:n.*50A>C
NM_001276504.2:c.336A>C	NP_001263433.1:p.Lys112Asn
NM_001276506.2:c.*151A>C	NP_001263435.1:n.*151A>C
NR_077060.2:n.542A>C