Canonical Allele Identifier: CA1521983254
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.236497_236498delinsGC , CM000667.2:g.236497_236498delinsGC GRCh38
NC_000005.9:g.236612_236613delinsGC , CM000667.1:g.236612_236613delinsGC GRCh37
NC_000005.8:g.289612_289613delinsGC NCBI36
NG_012339.1:g.23257_23258delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.1330_1331delinsGC MANE Select ENSP00000264932.6:p.Ala444=
ENST00000651543.1:c.*63_*64delinsGC ENSP00000499215.1:n.*63_*64delinsGC
ENST00000264932.10:c.1330_1331delinsGC ENSP00000264932.6:p.Ala444=
ENST00000504309.5:c.1330_1331delinsGC ENSP00000426514.1:p.Ala444=
ENST00000505555.5:n.1370_1371delinsGC
ENST00000510361.5:c.1186_1187delinsGC ENSP00000427703.1:p.Ala396=
ENST00000511810.5:n.2077_2078delinsGC
ENST00000512962.5:n.916_917delinsGC
ENST00000514027.5:n.1285_1286delinsGC
ENST00000515752.5:n.916_917delinsGC
ENST00000617470.4:c.895_896delinsGC ENSP00000484230.1:p.Ala299=
NM_001294332.1:c.1186_1187delinsGC NP_001281261.1:p.Ala396=
NM_004168.3:c.1330_1331delinsGC NP_004159.2:p.Ala444=
XM_005248331.2:c.1330_1331delinsGC XP_005248388.1:p.Ala444=
XM_011514072.1:c.1330_1331delinsGC XP_011512374.1:p.Ala444=
XM_011514073.1:c.1330_1331delinsGC XP_011512375.1:p.Ala444=
XR_925638.1:n.1463_1464delinsGC
NM_001330758.1:c.1330_1331delinsGC NP_001317687.1:p.Ala444=
XM_011514072.2:c.1330_1331delinsGC XP_011512374.1:p.Ala444=
XM_011514073.2:c.1330_1331delinsGC XP_011512375.1:p.Ala444=
XM_017009685.2:c.1330_1331delinsGC XP_016865174.1:p.Ala444=
XM_024446143.1:c.1186_1187delinsGC XP_024301911.1:p.Ala396=
XR_002956167.1:n.1377_1378delinsGC
NM_004168.4:c.1330_1331delinsGC MANE Select NP_004159.2:p.Ala444=
NM_001294332.2:c.1186_1187delinsGC NP_001281261.1:p.Ala396=
NM_001330758.2:c.1330_1331delinsGC NP_001317687.1:p.Ala444=