Canonical Allele Identifier: CA359012672
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.233536A>G , CM000667.2:g.233536A>G GRCh38
NC_000005.9:g.233651A>G , CM000667.1:g.233651A>G GRCh37
NC_000005.8:g.286651A>G NCBI36
NG_012339.1:g.20296A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004168.4:c.955A>G MANE Select NP_004159.2:p.Ile319Val
ENST00000264932.11:c.955A>G MANE Select ENSP00000264932.6:p.Ile319Val
NM_001294332.1:c.811A>G NP_001281261.1:p.Ile271Val
NM_001294332.2:c.811A>G NP_001281261.1:p.Ile271Val
NM_001330758.1:c.955A>G NP_001317687.1:p.Ile319Val
NM_001330758.2:c.955A>G NP_001317687.1:p.Ile319Val
NM_004168.3:c.955A>G NP_004159.2:p.Ile319Val
ENST00000264932.10:c.955A>G ENSP00000264932.6:p.Ile319Val
ENST00000504309.5:c.955A>G ENSP00000426514.1:p.Ile319Val
ENST00000504824.5:n.940A>G
ENST00000505555.5:n.995A>G
ENST00000510361.5:c.811A>G ENSP00000427703.1:p.Ile271Val
ENST00000512962.5:n.118A>G
ENST00000514027.5:n.910A>G
ENST00000514233.1:n.465A>G
ENST00000515752.5:n.118A>G
ENST00000617470.4:c.520A>G ENSP00000484230.1:p.Ile174Val
ENST00000651543.1:c.955A>G ENSP00000499215.1:p.Ile319Val
XM_005248331.2:c.955A>G XP_005248388.1:p.Ile319Val
XM_011514072.1:c.955A>G XP_011512374.1:p.Ile319Val
XM_011514072.2:c.955A>G XP_011512374.1:p.Ile319Val
XM_011514073.1:c.955A>G XP_011512375.1:p.Ile319Val
XM_011514073.2:c.955A>G XP_011512375.1:p.Ile319Val
XM_017009685.2:c.955A>G XP_016865174.1:p.Ile319Val
XM_024446143.1:c.811A>G XP_024301911.1:p.Ile271Val
XR_002956167.1:n.1002A>G
XR_925638.1:n.1088A>G