Canonical Allele Identifier: CA1521982853
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.225204_225206delinsCTG , CM000667.2:g.225204_225206delinsCTG GRCh38
NC_000005.9:g.225319_225321delinsCTG , CM000667.1:g.225319_225321delinsCTG GRCh37
NC_000005.8:g.278319_278321delinsCTG NCBI36
NG_012339.1:g.11964_11966delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.313-215_313-213delinsCTG MANE Select ENSP00000264932.6:n.313-215_313-213delinsCTG
ENST00000651543.1:c.313-215_313-213delinsCTG ENSP00000499215.1:n.313-215_313-213delinsCTG
ENST00000264932.10:c.313-215_313-213delinsCTG ENSP00000264932.6:n.313-215_313-213delinsCTG
ENST00000504309.5:c.313-215_313-213delinsCTG ENSP00000426514.1:n.313-215_313-213delinsCTG
ENST00000504824.5:n.298-215_298-213delinsCTG
ENST00000505555.5:n.353-215_353-213delinsCTG
ENST00000509632.5:c.*141-215_*141-213delinsCTG ENSP00000425077.1:n.*141-215_*141-213delinsCTG
ENST00000510361.5:c.313-679_313-677delinsCTG ENSP00000427703.1:n.313-679_313-677delinsCTG
ENST00000617470.4:c.313-215_313-213delinsCTG ENSP00000484230.1:n.313-215_313-213delinsCTG
NM_001294332.1:c.313-679_313-677delinsCTG NP_001281261.1:n.313-679_313-677delinsCTG
NM_004168.3:c.313-215_313-213delinsCTG NP_004159.2:n.313-215_313-213delinsCTG
XM_005248331.2:c.313-215_313-213delinsCTG XP_005248388.1:n.313-215_313-213delinsCTG
XM_011514072.1:c.313-215_313-213delinsCTG XP_011512374.1:n.313-215_313-213delinsCTG
XM_011514073.1:c.313-215_313-213delinsCTG XP_011512375.1:n.313-215_313-213delinsCTG
XR_925638.1:n.446-215_446-213delinsCTG
NM_001330758.1:c.313-215_313-213delinsCTG NP_001317687.1:n.313-215_313-213delinsCTG
XM_011514072.2:c.313-215_313-213delinsCTG XP_011512374.1:n.313-215_313-213delinsCTG
XM_011514073.2:c.313-215_313-213delinsCTG XP_011512375.1:n.313-215_313-213delinsCTG
XM_017009685.2:c.313-215_313-213delinsCTG XP_016865174.1:n.313-215_313-213delinsCTG
XM_024446143.1:c.313-679_313-677delinsCTG XP_024301911.1:n.313-679_313-677delinsCTG
XR_002956167.1:n.360-215_360-213delinsCTG
NM_004168.4:c.313-215_313-213delinsCTG MANE Select NP_004159.2:n.313-215_313-213delinsCTG
NM_001294332.2:c.313-679_313-677delinsCTG NP_001281261.1:n.313-679_313-677delinsCTG
NM_001330758.2:c.313-215_313-213delinsCTG NP_001317687.1:n.313-215_313-213delinsCTG