Canonical Allele Identifier: CA442690951
Gene: SDHA HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.225539A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.225424A>C , CM000667.2:g.225424A>C GRCh38
NC_000005.9:g.225539A>C , CM000667.1:g.225539A>C GRCh37
NC_000005.8:g.278539A>C NCBI36
NG_012339.1:g.12184A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.318A>C MANE Select ENSP00000264932.6:p.Gly106=
ENST00000651543.1:c.318A>C ENSP00000499215.1:p.Gly106=
ENST00000264932.10:c.318A>C ENSP00000264932.6:p.Gly106=
ENST00000504309.5:c.318A>C ENSP00000426514.1:p.Gly106=
ENST00000504824.5:n.303A>C
ENST00000505555.5:n.358A>C
ENST00000509632.5:c.*146A>C ENSP00000425077.1:n.*146A>C
ENST00000510361.5:c.313-459A>C ENSP00000427703.1:n.313-459A>C
ENST00000617470.4:c.318A>C ENSP00000484230.1:p.Gly106=
NM_001294332.1:c.313-459A>C NP_001281261.1:n.313-459A>C
NM_004168.3:c.318A>C NP_004159.2:p.Gly106=
XM_005248331.2:c.318A>C XP_005248388.1:p.Gly106=
XM_011514072.1:c.318A>C XP_011512374.1:p.Gly106=
XM_011514073.1:c.318A>C XP_011512375.1:p.Gly106=
XR_925638.1:n.451A>C
NM_001330758.1:c.318A>C NP_001317687.1:p.Gly106=
XM_011514072.2:c.318A>C XP_011512374.1:p.Gly106=
XM_011514073.2:c.318A>C XP_011512375.1:p.Gly106=
XM_017009685.2:c.318A>C XP_016865174.1:p.Gly106=
XM_024446143.1:c.313-459A>C XP_024301911.1:n.313-459A>C
XR_002956167.1:n.365A>C
NM_004168.4:c.318A>C MANE Select NP_004159.2:p.Gly106=
NM_001294332.2:c.313-459A>C NP_001281261.1:n.313-459A>C
NM_001330758.2:c.318A>C NP_001317687.1:p.Gly106=