Canonical Allele Identifier: CA1521983628
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.236591G= , CM000667.2:g.236591G= GRCh38
NC_000005.9:g.236706G= , CM000667.1:g.236706G= GRCh37
NC_000005.8:g.289706G= NCBI36
NG_012339.1:g.23351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.1424G= MANE Select ENSP00000264932.6:p.Cys475=
ENST00000651543.1:c.*157G= ENSP00000499215.1:n.*157G=
ENST00000264932.10:c.1424G= ENSP00000264932.6:p.Cys475=
ENST00000504309.5:c.1424G= ENSP00000426514.1:p.Cys475=
ENST00000505555.5:n.1464G=
ENST00000510361.5:c.1280G= ENSP00000427703.1:p.Cys427=
ENST00000511810.5:n.2171G=
ENST00000514027.5:n.1379G=
ENST00000515752.5:n.1010G=
ENST00000515815.5:c.79G=
ENST00000617470.4:c.989G= ENSP00000484230.1:p.Cys330=
NM_001294332.1:c.1280G= NP_001281261.1:p.Cys427=
NM_004168.3:c.1424G= NP_004159.2:p.Cys475=
XM_005248331.2:c.1424G= XP_005248388.1:p.Cys475=
XM_011514072.1:c.1424G= XP_011512374.1:p.Cys475=
XM_011514073.1:c.1424G= XP_011512375.1:p.Cys475=
XR_925638.1:n.1557G=
NM_001330758.1:c.1424G= NP_001317687.1:p.Cys475=
XM_011514072.2:c.1424G= XP_011512374.1:p.Cys475=
XM_011514073.2:c.1424G= XP_011512375.1:p.Cys475=
XM_017009685.2:c.1424G= XP_016865174.1:p.Cys475=
XM_024446143.1:c.1280G= XP_024301911.1:p.Cys427=
XR_002956167.1:n.1471G=
NM_004168.4:c.1424G= MANE Select NP_004159.2:p.Cys475=
NM_001294332.2:c.1280G= NP_001281261.1:p.Cys427=
NM_001330758.2:c.1424G= NP_001317687.1:p.Cys475=