Canonical Allele Identifier: CA915943270

Gene: SDHA

Linked Data

• ClinVar Variation Id: 765632
• ClinVar RCV Id: RCV001419853
• dbSNP Id: rs1579417426

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.240349T>C , CM000667.2:g.240349T>C	GRCh38
NC_000005.9:g.240464T>C , CM000667.1:g.240464T>C	GRCh37
NC_000005.8:g.293464T>C	NCBI36
NG_012339.1:g.27109T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1433-9T>C MANE Select	ENSP00000264932.6:n.1433-9T>C
ENST00000651543.1:c.*166-9T>C	ENSP00000499215.1:n.*166-9T>C
ENST00000264932.10:c.1433-9T>C	ENSP00000264932.6:n.1433-9T>C
ENST00000504309.5:c.1433-9T>C	ENSP00000426514.1:n.1433-9T>C
ENST00000505555.5:n.1473-9T>C
ENST00000510361.5:c.1289-9T>C	ENSP00000427703.1:n.1289-9T>C
ENST00000511810.5:n.2180-9T>C
ENST00000514027.5:n.1388-9T>C
ENST00000515752.5:n.1019-9T>C
ENST00000515815.5:c.88-9T>C
ENST00000617470.4:c.998-9T>C	ENSP00000484230.1:n.998-9T>C
NM_001294332.1:c.1289-9T>C	NP_001281261.1:n.1289-9T>C
NM_004168.3:c.1433-9T>C	NP_004159.2:n.1433-9T>C
XM_005248331.2:c.1433-9T>C	XP_005248388.1:n.1433-9T>C
XM_011514072.1:c.1433-9T>C	XP_011512374.1:n.1433-9T>C
XM_011514073.1:c.1433-9T>C	XP_011512375.1:n.1433-9T>C
XR_925638.1:n.1566-9T>C
NM_001330758.1:c.1433-9T>C	NP_001317687.1:n.1433-9T>C
XM_011514072.2:c.1433-9T>C	XP_011512374.1:n.1433-9T>C
XM_011514073.2:c.1433-9T>C	XP_011512375.1:n.1433-9T>C
XM_017009685.2:c.1433-9T>C	XP_016865174.1:n.1433-9T>C
XM_024446143.1:c.1289-9T>C	XP_024301911.1:n.1289-9T>C
XR_002956167.1:n.1480-9T>C
NM_004168.4:c.1433-9T>C MANE Select	NP_004159.2:n.1433-9T>C
NM_001294332.2:c.1289-9T>C	NP_001281261.1:n.1289-9T>C
NM_001330758.2:c.1433-9T>C	NP_001317687.1:n.1433-9T>C