Canonical Allele Identifier: CA359009908
Gene: SDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.225902C>G , CM000667.2:g.225902C>G GRCh38
NC_000005.9:g.226017C>G , CM000667.1:g.226017C>G GRCh37
NC_000005.8:g.279017C>G NCBI36
NG_012339.1:g.12662C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.476C>G MANE Select ENSP00000264932.6:p.Pro159Arg
ENST00000651543.1:c.476C>G ENSP00000499215.1:p.Pro159Arg
ENST00000264932.10:c.476C>G ENSP00000264932.6:p.Pro159Arg
ENST00000504309.5:c.476C>G ENSP00000426514.1:p.Pro159Arg
ENST00000504824.5:n.461C>G
ENST00000505555.5:n.516C>G
ENST00000509420.5:n.270C>G
ENST00000510361.5:c.332C>G ENSP00000427703.1:p.Pro111Arg
ENST00000617470.4:c.380+416C>G ENSP00000484230.1:n.380+416C>G
NM_001294332.1:c.332C>G NP_001281261.1:p.Pro111Arg
NM_004168.3:c.476C>G NP_004159.2:p.Pro159Arg
XM_005248331.2:c.476C>G XP_005248388.1:p.Pro159Arg
XM_011514072.1:c.476C>G XP_011512374.1:p.Pro159Arg
XM_011514073.1:c.476C>G XP_011512375.1:p.Pro159Arg
XR_925638.1:n.609C>G
NM_001330758.1:c.476C>G NP_001317687.1:p.Pro159Arg
XM_011514072.2:c.476C>G XP_011512374.1:p.Pro159Arg
XM_011514073.2:c.476C>G XP_011512375.1:p.Pro159Arg
XM_017009685.2:c.476C>G XP_016865174.1:p.Pro159Arg
XM_024446143.1:c.332C>G XP_024301911.1:p.Pro111Arg
XR_002956167.1:n.523C>G
NM_004168.4:c.476C>G MANE Select NP_004159.2:p.Pro159Arg
NM_001294332.2:c.332C>G NP_001281261.1:p.Pro111Arg
NM_001330758.2:c.476C>G NP_001317687.1:p.Pro159Arg