Canonical Allele Identifier: CA1521984364
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.225895G= , CM000667.2:g.225895G= GRCh38
NC_000005.9:g.226010G= , CM000667.1:g.226010G= GRCh37
NC_000005.8:g.279010G= NCBI36
NG_012339.1:g.12655G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.469G= MANE Select ENSP00000264932.6:p.Gly157=
ENST00000651543.1:c.469G= ENSP00000499215.1:p.Gly157=
ENST00000264932.10:c.469G= ENSP00000264932.6:p.Gly157=
ENST00000504309.5:c.469G= ENSP00000426514.1:p.Gly157=
ENST00000504824.5:n.454G=
ENST00000505555.5:n.509G=
ENST00000509420.5:n.263G=
ENST00000510361.5:c.325G= ENSP00000427703.1:p.Gly109=
ENST00000617470.4:c.380+409G= ENSP00000484230.1:n.380+409G=
NM_001294332.1:c.325G= NP_001281261.1:p.Gly109=
NM_004168.3:c.469G= NP_004159.2:p.Gly157=
XM_005248331.2:c.469G= XP_005248388.1:p.Gly157=
XM_011514072.1:c.469G= XP_011512374.1:p.Gly157=
XM_011514073.1:c.469G= XP_011512375.1:p.Gly157=
XR_925638.1:n.602G=
NM_001330758.1:c.469G= NP_001317687.1:p.Gly157=
XM_011514072.2:c.469G= XP_011512374.1:p.Gly157=
XM_011514073.2:c.469G= XP_011512375.1:p.Gly157=
XM_017009685.2:c.469G= XP_016865174.1:p.Gly157=
XM_024446143.1:c.325G= XP_024301911.1:p.Gly109=
XR_002956167.1:n.516G=
NM_004168.4:c.469G= MANE Select NP_004159.2:p.Gly157=
NM_001294332.2:c.325G= NP_001281261.1:p.Gly109=
NM_001330758.2:c.469G= NP_001317687.1:p.Gly157=