Canonical Allele Identifier: CA359014282
Gene: SDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.240415A>C , CM000667.2:g.240415A>C GRCh38
NC_000005.9:g.240530A>C , CM000667.1:g.240530A>C GRCh37
NC_000005.8:g.293530A>C NCBI36
NG_012339.1:g.27175A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.1490A>C MANE Select ENSP00000264932.6:p.Asp497Ala
ENST00000651543.1:c.*223A>C ENSP00000499215.1:n.*223A>C
ENST00000264932.10:c.1490A>C ENSP00000264932.6:p.Asp497Ala
ENST00000504309.5:c.1490A>C ENSP00000426514.1:p.Asp497Ala
ENST00000505555.5:n.1530A>C
ENST00000510361.5:c.1346A>C ENSP00000427703.1:p.Asp449Ala
ENST00000511810.5:n.2237A>C
ENST00000514027.5:n.1445A>C
ENST00000515752.5:n.1076A>C
ENST00000515815.5:c.145A>C
ENST00000617470.4:c.1055A>C ENSP00000484230.1:p.Asp352Ala
NM_001294332.1:c.1346A>C NP_001281261.1:p.Asp449Ala
NM_004168.3:c.1490A>C NP_004159.2:p.Asp497Ala
XM_005248331.2:c.1490A>C XP_005248388.1:p.Asp497Ala
XM_011514072.1:c.1490A>C XP_011512374.1:p.Asp497Ala
XM_011514073.1:c.1490A>C XP_011512375.1:p.Asp497Ala
XR_925638.1:n.1623A>C
NM_001330758.1:c.1490A>C NP_001317687.1:p.Asp497Ala
XM_011514072.2:c.1490A>C XP_011512374.1:p.Asp497Ala
XM_011514073.2:c.1490A>C XP_011512375.1:p.Asp497Ala
XM_017009685.2:c.1490A>C XP_016865174.1:p.Asp497Ala
XM_024446143.1:c.1346A>C XP_024301911.1:p.Asp449Ala
XR_002956167.1:n.1537A>C
NM_004168.4:c.1490A>C MANE Select NP_004159.2:p.Asp497Ala
NM_001294332.2:c.1346A>C NP_001281261.1:p.Asp449Ala
NM_001330758.2:c.1490A>C NP_001317687.1:p.Asp497Ala