Canonical Allele Identifier: CA3173189

Gene: SDHA

Linked Data

• ClinVar Variation Id: 937480
• ClinVar RCV Id: RCV001206499 ; RCV002379782
• dbSNP Id: rs772729820
• ExAC: 5:236588 T / C
• gnomAD v3: 5-236473-T-C
• gnomAD v4: 5-236473-T-C
• MyVariant Identifiers: chr5:g.236588T>C (hg19) ; chr5:g.236473T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236473T>C , CM000667.2:g.236473T>C	GRCh38
NC_000005.9:g.236588T>C , CM000667.1:g.236588T>C	GRCh37
NC_000005.8:g.289588T>C	NCBI36
NG_012339.1:g.23233T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1306T>C MANE Select	ENSP00000264932.6:p.Tyr436His
ENST00000651543.1:c.*39T>C	ENSP00000499215.1:n.*39T>C
ENST00000264932.10:c.1306T>C	ENSP00000264932.6:p.Tyr436His
ENST00000504309.5:c.1306T>C	ENSP00000426514.1:p.Tyr436His
ENST00000505555.5:n.1346T>C
ENST00000510361.5:c.1162T>C	ENSP00000427703.1:p.Tyr388His
ENST00000511810.5:n.2053T>C
ENST00000512962.5:n.892T>C
ENST00000514027.5:n.1261T>C
ENST00000515752.5:n.892T>C
ENST00000617470.4:c.871T>C	ENSP00000484230.1:p.Tyr291His
NM_001294332.1:c.1162T>C	NP_001281261.1:p.Tyr388His
NM_004168.3:c.1306T>C	NP_004159.2:p.Tyr436His
XM_005248331.2:c.1306T>C	XP_005248388.1:p.Tyr436His
XM_011514072.1:c.1306T>C	XP_011512374.1:p.Tyr436His
XM_011514073.1:c.1306T>C	XP_011512375.1:p.Tyr436His
XR_925638.1:n.1439T>C
NM_001330758.1:c.1306T>C	NP_001317687.1:p.Tyr436His
XM_011514072.2:c.1306T>C	XP_011512374.1:p.Tyr436His
XM_011514073.2:c.1306T>C	XP_011512375.1:p.Tyr436His
XM_017009685.2:c.1306T>C	XP_016865174.1:p.Tyr436His
XM_024446143.1:c.1162T>C	XP_024301911.1:p.Tyr388His
XR_002956167.1:n.1353T>C
NM_004168.4:c.1306T>C MANE Select	NP_004159.2:p.Tyr436His
NM_001294332.2:c.1162T>C	NP_001281261.1:p.Tyr388His
NM_001330758.2:c.1306T>C	NP_001317687.1:p.Tyr436His