Canonical Allele Identifier: CA476790981

Gene: SDHD

Linked Data

• ClinVar Variation Id: 1739783
• ClinVar RCV Id: RCV002332120
• gnomAD v4: 11-112094922-T-C
• MyVariant Identifiers: chr11:g.111965646T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094922T>C , CM000673.2:g.112094922T>C	GRCh38
NC_000011.9:g.111965646T>C , CM000673.1:g.111965646T>C	GRCh37
NC_000011.8:g.111470856T>C	NCBI36
NG_012337.2:g.13076T>C
NG_012337.3:g.13076T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*171T>C	ENSP00000432946.2:n.*171T>C
ENST00000534010.2:c.314+5911T>C	ENSP00000433202.2:n.314+5911T>C
ENST00000375549.8:c.432T>C MANE Select	ENSP00000364699.3:p.Tyr144=
ENST00000528021.6:c.314+5911T>C	ENSP00000432465.1:n.314+5911T>C
ENST00000375549.7:c.432T>C	ENSP00000364699.3:p.Tyr144=
ENST00000525291.5:c.315T>C	ENSP00000436669.1:p.Tyr105=
ENST00000525987.5:n.319+5911T>C
ENST00000526592.5:c.*130T>C	ENSP00000432005.1:n.*130T>C
ENST00000528021.5:c.314+5911T>C	ENSP00000432465.1:n.314+5911T>C
ENST00000528048.5:c.*29T>C	ENSP00000436217.1:n.*29T>C
ENST00000528182.5:c.*29T>C	ENSP00000435475.1:n.*29T>C
ENST00000530923.5:c.476T>C
ENST00000531744.5:c.314+5911T>C	ENSP00000456957.1:n.314+5911T>C
ENST00000532699.1:c.314+5911T>C	ENSP00000456434.1:n.314+5911T>C
ENST00000534010.1:c.145+5911T>C
NM_001276503.1:c.*29T>C	NP_001263432.1:n.*29T>C
NM_001276504.1:c.315T>C	NP_001263433.1:p.Tyr105=
NM_001276506.1:c.*130T>C	NP_001263435.1:n.*130T>C
NM_003002.3:c.432T>C	NP_002993.1:p.Tyr144=
NR_077060.1:n.570T>C
NM_003002.4:c.432T>C MANE Select	NP_002993.1:p.Tyr144=
NM_001276503.2:c.*29T>C	NP_001263432.1:n.*29T>C
NM_001276504.2:c.315T>C	NP_001263433.1:p.Tyr105=
NM_001276506.2:c.*130T>C	NP_001263435.1:n.*130T>C
NR_077060.2:n.521T>C