Canonical Allele Identifier: CA359013910

Gene: SDHA

Linked Data

• ClinVar Variation Id: 933488
• ClinVar RCV Id: RCV001201712
• dbSNP Id: rs1579409601
• MyVariant Identifiers: chr5:g.236597G>A (hg19) ; chr5:g.236482G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236482G>A , CM000667.2:g.236482G>A	GRCh38
NC_000005.9:g.236597G>A , CM000667.1:g.236597G>A	GRCh37
NC_000005.8:g.289597G>A	NCBI36
NG_012339.1:g.23242G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1315G>A MANE Select	ENSP00000264932.6:p.Gly439Arg
ENST00000651543.1:c.*48G>A	ENSP00000499215.1:n.*48G>A
ENST00000264932.10:c.1315G>A	ENSP00000264932.6:p.Gly439Arg
ENST00000504309.5:c.1315G>A	ENSP00000426514.1:p.Gly439Arg
ENST00000505555.5:n.1355G>A
ENST00000510361.5:c.1171G>A	ENSP00000427703.1:p.Gly391Arg
ENST00000511810.5:n.2062G>A
ENST00000512962.5:n.901G>A
ENST00000514027.5:n.1270G>A
ENST00000515752.5:n.901G>A
ENST00000617470.4:c.880G>A	ENSP00000484230.1:p.Gly294Arg
NM_001294332.1:c.1171G>A	NP_001281261.1:p.Gly391Arg
NM_004168.3:c.1315G>A	NP_004159.2:p.Gly439Arg
XM_005248331.2:c.1315G>A	XP_005248388.1:p.Gly439Arg
XM_011514072.1:c.1315G>A	XP_011512374.1:p.Gly439Arg
XM_011514073.1:c.1315G>A	XP_011512375.1:p.Gly439Arg
XR_925638.1:n.1448G>A
NM_001330758.1:c.1315G>A	NP_001317687.1:p.Gly439Arg
XM_011514072.2:c.1315G>A	XP_011512374.1:p.Gly439Arg
XM_011514073.2:c.1315G>A	XP_011512375.1:p.Gly439Arg
XM_017009685.2:c.1315G>A	XP_016865174.1:p.Gly439Arg
XM_024446143.1:c.1171G>A	XP_024301911.1:p.Gly391Arg
XR_002956167.1:n.1362G>A
NM_004168.4:c.1315G>A MANE Select	NP_004159.2:p.Gly439Arg
NM_001294332.2:c.1171G>A	NP_001281261.1:p.Gly391Arg
NM_001330758.2:c.1315G>A	NP_001317687.1:p.Gly439Arg