Canonical Allele Identifier: CA1072366318
Gene: SDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.240359_240360insTTTT , CM000667.2:g.240359_240360insTTTT GRCh38
NC_000005.9:g.240474_240475insTTTT , CM000667.1:g.240474_240475insTTTT GRCh37
NC_000005.8:g.293474_293475insTTTT NCBI36
NG_012339.1:g.27119_27120insTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.1434_1435insTTTT MANE Select ENSP00000264932.6:p.Asp479PhefsTer2
ENST00000651543.1:c.*167_*168insTTTT ENSP00000499215.1:n.*167_*168insTTTT
ENST00000264932.10:c.1434_1435insTTTT ENSP00000264932.6:p.Asp479PhefsTer2
ENST00000504309.5:c.1434_1435insTTTT ENSP00000426514.1:p.Asp479PhefsTer2
ENST00000505555.5:n.1474_1475insTTTT
ENST00000510361.5:c.1290_1291insTTTT ENSP00000427703.1:p.Asp431PhefsTer2
ENST00000511810.5:n.2181_2182insTTTT
ENST00000514027.5:n.1389_1390insTTTT
ENST00000515752.5:n.1020_1021insTTTT
ENST00000515815.5:c.89_90insTTTT
ENST00000617470.4:c.999_1000insTTTT ENSP00000484230.1:p.Asp334PhefsTer2
NM_001294332.1:c.1290_1291insTTTT NP_001281261.1:p.Asp431PhefsTer2
NM_004168.3:c.1434_1435insTTTT NP_004159.2:p.Asp479PhefsTer2
XM_005248331.2:c.1434_1435insTTTT XP_005248388.1:p.Asp479PhefsTer2
XM_011514072.1:c.1434_1435insTTTT XP_011512374.1:p.Asp479PhefsTer2
XM_011514073.1:c.1434_1435insTTTT XP_011512375.1:p.Asp479PhefsTer2
XR_925638.1:n.1567_1568insTTTT
NM_001330758.1:c.1434_1435insTTTT NP_001317687.1:p.Asp479PhefsTer2
XM_011514072.2:c.1434_1435insTTTT XP_011512374.1:p.Asp479PhefsTer2
XM_011514073.2:c.1434_1435insTTTT XP_011512375.1:p.Asp479PhefsTer2
XM_017009685.2:c.1434_1435insTTTT XP_016865174.1:p.Asp479PhefsTer2
XM_024446143.1:c.1290_1291insTTTT XP_024301911.1:p.Asp431PhefsTer2
XR_002956167.1:n.1481_1482insTTTT
NM_004168.4:c.1434_1435insTTTT MANE Select NP_004159.2:p.Asp479PhefsTer2
NM_001294332.2:c.1290_1291insTTTT NP_001281261.1:p.Asp431PhefsTer2
NM_001330758.2:c.1434_1435insTTTT NP_001317687.1:p.Asp479PhefsTer2