Canonical Allele Identifier: CA1521982997
Gene: SDHA HGNC NCBI

Linked Data

dbSNP Id: rs1735781019

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.236439_236440insA , CM000667.2:g.236439_236440insA GRCh38
NC_000005.9:g.236554_236555insA , CM000667.1:g.236554_236555insA GRCh37
NC_000005.8:g.289554_289555insA NCBI36
NG_012339.1:g.23199_23200insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.1272_1273insA MANE Select ENSP00000264932.6:p.Val425SerfsTer?
ENST00000651543.1:c.*5_*6insA ENSP00000499215.1:n.*5_*6insA
ENST00000264932.10:c.1272_1273insA ENSP00000264932.6:p.Val425SerfsTer?
ENST00000504309.5:c.1272_1273insA ENSP00000426514.1:p.Val425SerfsTer?
ENST00000505555.5:n.1312_1313insA
ENST00000510361.5:c.1128_1129insA ENSP00000427703.1:p.Val377SerfsTer?
ENST00000511810.5:n.2019_2020insA
ENST00000512962.5:n.858_859insA
ENST00000514027.5:n.1227_1228insA
ENST00000515752.5:n.858_859insA
ENST00000617470.4:c.837_838insA ENSP00000484230.1:p.Val280SerfsTer?
NM_001294332.1:c.1128_1129insA NP_001281261.1:p.Val377SerfsTer?
NM_004168.3:c.1272_1273insA NP_004159.2:p.Val425SerfsTer?
XM_005248331.2:c.1272_1273insA XP_005248388.1:p.Val425SerfsTer?
XM_011514072.1:c.1272_1273insA XP_011512374.1:p.Val425SerfsTer?
XM_011514073.1:c.1272_1273insA XP_011512375.1:p.Val425SerfsTer?
XR_925638.1:n.1405_1406insA
NM_001330758.1:c.1272_1273insA NP_001317687.1:p.Val425SerfsTer?
XM_011514072.2:c.1272_1273insA XP_011512374.1:p.Val425SerfsTer?
XM_011514073.2:c.1272_1273insA XP_011512375.1:p.Val425SerfsTer?
XM_017009685.2:c.1272_1273insA XP_016865174.1:p.Val425SerfsTer?
XM_024446143.1:c.1128_1129insA XP_024301911.1:p.Val377SerfsTer?
XR_002956167.1:n.1319_1320insA
NM_004168.4:c.1272_1273insA MANE Select NP_004159.2:p.Val425SerfsTer?
NM_001294332.2:c.1128_1129insA NP_001281261.1:p.Val377SerfsTer?
NM_001330758.2:c.1272_1273insA NP_001317687.1:p.Val425SerfsTer?