Canonical Allele Identifier: CA359014150

Gene: SDHA

Linked Data

• ClinVar Variation Id: 2011312
• ClinVar RCV Id: RCV002851247
• MyVariant Identifiers: chr5:g.240471A>G (hg19) ; chr5:g.240356A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.240356A>G , CM000667.2:g.240356A>G	GRCh38
NC_000005.9:g.240471A>G , CM000667.1:g.240471A>G	GRCh37
NC_000005.8:g.293471A>G	NCBI36
NG_012339.1:g.27116A>G

Transcript Alleles

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