Canonical Allele Identifier: CA1521988016
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.240363A= , CM000667.2:g.240363A= GRCh38
NC_000005.9:g.240478A= , CM000667.1:g.240478A= GRCh37
NC_000005.8:g.293478A= NCBI36
NG_012339.1:g.27123A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264932.11:c.1438A= MANE Select ENSP00000264932.6:p.Lys480=
ENST00000651543.1:c.*171A= ENSP00000499215.1:n.*171A=
ENST00000264932.10:c.1438A= ENSP00000264932.6:p.Lys480=
ENST00000504309.5:c.1438A= ENSP00000426514.1:p.Lys480=
ENST00000505555.5:n.1478A=
ENST00000510361.5:c.1294A= ENSP00000427703.1:p.Lys432=
ENST00000511810.5:n.2185A=
ENST00000514027.5:n.1393A=
ENST00000515752.5:n.1024A=
ENST00000515815.5:c.93A=
ENST00000617470.4:c.1003A= ENSP00000484230.1:p.Lys335=
NM_001294332.1:c.1294A= NP_001281261.1:p.Lys432=
NM_004168.3:c.1438A= NP_004159.2:p.Lys480=
XM_005248331.2:c.1438A= XP_005248388.1:p.Lys480=
XM_011514072.1:c.1438A= XP_011512374.1:p.Lys480=
XM_011514073.1:c.1438A= XP_011512375.1:p.Lys480=
XR_925638.1:n.1571A=
NM_001330758.1:c.1438A= NP_001317687.1:p.Lys480=
XM_011514072.2:c.1438A= XP_011512374.1:p.Lys480=
XM_011514073.2:c.1438A= XP_011512375.1:p.Lys480=
XM_017009685.2:c.1438A= XP_016865174.1:p.Lys480=
XM_024446143.1:c.1294A= XP_024301911.1:p.Lys432=
XR_002956167.1:n.1485A=
NM_004168.4:c.1438A= MANE Select NP_004159.2:p.Lys480=
NM_001294332.2:c.1294A= NP_001281261.1:p.Lys432=
NM_001330758.2:c.1438A= NP_001317687.1:p.Lys480=