Canonical Allele Identifier: CA1521983283
Gene: SDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.225438_225439delinsTG , CM000667.2:g.225438_225439delinsTG GRCh38
NC_000005.9:g.225553_225554delinsTG , CM000667.1:g.225553_225554delinsTG GRCh37
NC_000005.8:g.278553_278554delinsTG NCBI36
NG_012339.1:g.12198_12199delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000264932.11:c.332_333delinsTG MANE Select ENSP00000264932.6:p.Leu111=
ENST00000651543.1:c.332_333delinsTG ENSP00000499215.1:p.Leu111=
ENST00000264932.10:c.332_333delinsTG ENSP00000264932.6:p.Leu111=
ENST00000504309.5:c.332_333delinsTG ENSP00000426514.1:p.Leu111=
ENST00000504824.5:n.317_318delinsTG
ENST00000505555.5:n.372_373delinsTG
ENST00000509632.5:c.*160_*161delinsTG ENSP00000425077.1:n.*160_*161delinsTG
ENST00000510361.5:c.313-445_313-444delinsTG ENSP00000427703.1:n.313-445_313-444delinsTG
ENST00000617470.4:c.332_333delinsTG ENSP00000484230.1:p.Leu111=
NM_001294332.1:c.313-445_313-444delinsTG NP_001281261.1:n.313-445_313-444delinsTG
NM_004168.3:c.332_333delinsTG NP_004159.2:p.Leu111=
XM_005248331.2:c.332_333delinsTG XP_005248388.1:p.Leu111=
XM_011514072.1:c.332_333delinsTG XP_011512374.1:p.Leu111=
XM_011514073.1:c.332_333delinsTG XP_011512375.1:p.Leu111=
XR_925638.1:n.465_466delinsTG
NM_001330758.1:c.332_333delinsTG NP_001317687.1:p.Leu111=
XM_011514072.2:c.332_333delinsTG XP_011512374.1:p.Leu111=
XM_011514073.2:c.332_333delinsTG XP_011512375.1:p.Leu111=
XM_017009685.2:c.332_333delinsTG XP_016865174.1:p.Leu111=
XM_024446143.1:c.313-445_313-444delinsTG XP_024301911.1:n.313-445_313-444delinsTG
XR_002956167.1:n.379_380delinsTG
NM_004168.4:c.332_333delinsTG MANE Select NP_004159.2:p.Leu111=
NM_001294332.2:c.313-445_313-444delinsTG NP_001281261.1:n.313-445_313-444delinsTG
NM_001330758.2:c.332_333delinsTG NP_001317687.1:p.Leu111=