Canonical Allele Identifier: CA359014243
Gene: SDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.240399T>A , CM000667.2:g.240399T>A GRCh38
NC_000005.9:g.240514T>A , CM000667.1:g.240514T>A GRCh37
NC_000005.8:g.293514T>A NCBI36
NG_012339.1:g.27159T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.1474T>A MANE Select ENSP00000264932.6:p.Ser492Thr
ENST00000651543.1:c.*207T>A ENSP00000499215.1:n.*207T>A
ENST00000264932.10:c.1474T>A ENSP00000264932.6:p.Ser492Thr
ENST00000504309.5:c.1474T>A ENSP00000426514.1:p.Ser492Thr
ENST00000505555.5:n.1514T>A
ENST00000510361.5:c.1330T>A ENSP00000427703.1:p.Ser444Thr
ENST00000511810.5:n.2221T>A
ENST00000514027.5:n.1429T>A
ENST00000515752.5:n.1060T>A
ENST00000515815.5:c.129T>A
ENST00000617470.4:c.1039T>A ENSP00000484230.1:p.Ser347Thr
NM_001294332.1:c.1330T>A NP_001281261.1:p.Ser444Thr
NM_004168.3:c.1474T>A NP_004159.2:p.Ser492Thr
XM_005248331.2:c.1474T>A XP_005248388.1:p.Ser492Thr
XM_011514072.1:c.1474T>A XP_011512374.1:p.Ser492Thr
XM_011514073.1:c.1474T>A XP_011512375.1:p.Ser492Thr
XR_925638.1:n.1607T>A
NM_001330758.1:c.1474T>A NP_001317687.1:p.Ser492Thr
XM_011514072.2:c.1474T>A XP_011512374.1:p.Ser492Thr
XM_011514073.2:c.1474T>A XP_011512375.1:p.Ser492Thr
XM_017009685.2:c.1474T>A XP_016865174.1:p.Ser492Thr
XM_024446143.1:c.1330T>A XP_024301911.1:p.Ser444Thr
XR_002956167.1:n.1521T>A
NM_004168.4:c.1474T>A MANE Select NP_004159.2:p.Ser492Thr
NM_001294332.2:c.1330T>A NP_001281261.1:p.Ser444Thr
NM_001330758.2:c.1474T>A NP_001317687.1:p.Ser492Thr