Canonical Allele Identifier: CA1521983604
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.236582A= , CM000667.2:g.236582A= GRCh38
NC_000005.9:g.236697A= , CM000667.1:g.236697A= GRCh37
NC_000005.8:g.289697A= NCBI36
NG_012339.1:g.23342A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.1415A= MANE Select ENSP00000264932.6:p.Glu472=
ENST00000651543.1:c.*148A= ENSP00000499215.1:n.*148A=
ENST00000264932.10:c.1415A= ENSP00000264932.6:p.Glu472=
ENST00000504309.5:c.1415A= ENSP00000426514.1:p.Glu472=
ENST00000505555.5:n.1455A=
ENST00000510361.5:c.1271A= ENSP00000427703.1:p.Glu424=
ENST00000511810.5:n.2162A=
ENST00000514027.5:n.1370A=
ENST00000515752.5:n.1001A=
ENST00000515815.5:c.70A=
ENST00000617470.4:c.980A= ENSP00000484230.1:p.Glu327=
NM_001294332.1:c.1271A= NP_001281261.1:p.Glu424=
NM_004168.3:c.1415A= NP_004159.2:p.Glu472=
XM_005248331.2:c.1415A= XP_005248388.1:p.Glu472=
XM_011514072.1:c.1415A= XP_011512374.1:p.Glu472=
XM_011514073.1:c.1415A= XP_011512375.1:p.Glu472=
XR_925638.1:n.1548A=
NM_001330758.1:c.1415A= NP_001317687.1:p.Glu472=
XM_011514072.2:c.1415A= XP_011512374.1:p.Glu472=
XM_011514073.2:c.1415A= XP_011512375.1:p.Glu472=
XM_017009685.2:c.1415A= XP_016865174.1:p.Glu472=
XM_024446143.1:c.1271A= XP_024301911.1:p.Glu424=
XR_002956167.1:n.1462A=
NM_004168.4:c.1415A= MANE Select NP_004159.2:p.Glu472=
NM_001294332.2:c.1271A= NP_001281261.1:p.Glu424=
NM_001330758.2:c.1415A= NP_001317687.1:p.Glu472=