Canonical Allele Identifier: CA1521980710
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.223433G= , CM000667.2:g.223433G= GRCh38
NC_000005.9:g.223548G= , CM000667.1:g.223548G= GRCh37
NC_000005.8:g.276548G= NCBI36
NG_012339.1:g.10193G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264932.11:c.64-49G= MANE Select ENSP00000264932.6:n.64-49G=
ENST00000651543.1:c.64-49G= ENSP00000499215.1:n.64-49G=
ENST00000264932.10:c.64-49G= ENSP00000264932.6:n.64-49G=
ENST00000502379.5:n.109-49G=
ENST00000504309.5:c.64-49G= ENSP00000426514.1:n.64-49G=
ENST00000504824.5:n.49-49G=
ENST00000505555.5:n.104-49G=
ENST00000509632.5:c.162-49G= ENSP00000425077.1:n.162-49G=
ENST00000510361.5:c.64-49G= ENSP00000427703.1:n.64-49G=
ENST00000617470.4:c.64-49G= ENSP00000484230.1:n.64-49G=
NM_001294332.1:c.64-49G= NP_001281261.1:n.64-49G=
NM_004168.3:c.64-49G= NP_004159.2:n.64-49G=
XM_005248331.2:c.64-49G= XP_005248388.1:n.64-49G=
XM_011514072.1:c.64-49G= XP_011512374.1:n.64-49G=
XM_011514073.1:c.64-49G= XP_011512375.1:n.64-49G=
XR_925638.1:n.197-49G=
NM_001330758.1:c.64-49G= NP_001317687.1:n.64-49G=
XM_011514072.2:c.64-49G= XP_011512374.1:n.64-49G=
XM_011514073.2:c.64-49G= XP_011512375.1:n.64-49G=
XM_017009685.2:c.64-49G= XP_016865174.1:n.64-49G=
XM_024446143.1:c.64-49G= XP_024301911.1:n.64-49G=
XR_002956167.1:n.111-49G=
NM_004168.4:c.64-49G= MANE Select NP_004159.2:n.64-49G=
NM_001294332.2:c.64-49G= NP_001281261.1:n.64-49G=
NM_001330758.2:c.64-49G= NP_001317687.1:n.64-49G=