Canonical Allele Identifier: CA359009852
Gene: SDHA HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.469G>C MANE Select ENSP00000264932.6:p.Gly157Arg
ENST00000651543.1:c.469G>C ENSP00000499215.1:p.Gly157Arg
ENST00000264932.10:c.469G>C ENSP00000264932.6:p.Gly157Arg
ENST00000504309.5:c.469G>C ENSP00000426514.1:p.Gly157Arg
ENST00000504824.5:n.454G>C
ENST00000505555.5:n.509G>C
ENST00000509420.5:n.263G>C
ENST00000510361.5:c.325G>C ENSP00000427703.1:p.Gly109Arg
ENST00000617470.4:c.380+409G>C ENSP00000484230.1:n.380+409G>C
NM_001294332.1:c.325G>C NP_001281261.1:p.Gly109Arg
NM_004168.3:c.469G>C NP_004159.2:p.Gly157Arg
XM_005248331.2:c.469G>C XP_005248388.1:p.Gly157Arg
XM_011514072.1:c.469G>C XP_011512374.1:p.Gly157Arg
XM_011514073.1:c.469G>C XP_011512375.1:p.Gly157Arg
XR_925638.1:n.602G>C
NM_001330758.1:c.469G>C NP_001317687.1:p.Gly157Arg
XM_011514072.2:c.469G>C XP_011512374.1:p.Gly157Arg
XM_011514073.2:c.469G>C XP_011512375.1:p.Gly157Arg
XM_017009685.2:c.469G>C XP_016865174.1:p.Gly157Arg
XM_024446143.1:c.325G>C XP_024301911.1:p.Gly109Arg
XR_002956167.1:n.516G>C
NM_004168.4:c.469G>C MANE Select NP_004159.2:p.Gly157Arg
NM_001294332.2:c.325G>C NP_001281261.1:p.Gly109Arg
NM_001330758.2:c.469G>C NP_001317687.1:p.Gly157Arg