Canonical Allele Identifier: CA1521988109
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.240457T= , CM000667.2:g.240457T= GRCh38
NC_000005.9:g.240572T= , CM000667.1:g.240572T= GRCh37
NC_000005.8:g.293572T= NCBI36
NG_012339.1:g.27217T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264932.11:c.1532T= MANE Select ENSP00000264932.6:p.Leu511=
ENST00000651543.1:c.*265T= ENSP00000499215.1:n.*265T=
ENST00000264932.10:c.1532T= ENSP00000264932.6:p.Leu511=
ENST00000504309.5:c.1532T= ENSP00000426514.1:p.Leu511=
ENST00000505555.5:n.1572T=
ENST00000509082.1:n.14T=
ENST00000510361.5:c.1388T= ENSP00000427703.1:p.Leu463=
ENST00000511810.5:n.2279T=
ENST00000514027.5:n.1487T=
ENST00000515752.5:n.1118T=
ENST00000515815.5:c.187T=
ENST00000617470.4:c.1097T= ENSP00000484230.1:p.Leu366=
NM_001294332.1:c.1388T= NP_001281261.1:p.Leu463=
NM_004168.3:c.1532T= NP_004159.2:p.Leu511=
XM_005248331.2:c.1532T= XP_005248388.1:p.Leu511=
XM_011514072.1:c.1532T= XP_011512374.1:p.Leu511=
XM_011514073.1:c.1532T= XP_011512375.1:p.Leu511=
XR_925638.1:n.1665T=
NM_001330758.1:c.1532T= NP_001317687.1:p.Leu511=
XM_011514072.2:c.1532T= XP_011512374.1:p.Leu511=
XM_011514073.2:c.1532T= XP_011512375.1:p.Leu511=
XM_017009685.2:c.1532T= XP_016865174.1:p.Leu511=
XM_024446143.1:c.1388T= XP_024301911.1:p.Leu463=
XR_002956167.1:n.1579T=
NM_004168.4:c.1532T= MANE Select NP_004159.2:p.Leu511=
NM_001294332.2:c.1388T= NP_001281261.1:p.Leu463=
NM_001330758.2:c.1532T= NP_001317687.1:p.Leu511=