Canonical Allele Identifier: CA2672967028
Gene: SDHA HGNC NCBI

Linked Data

gnomAD v4: 5-225339-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.225339C>G , CM000667.2:g.225339C>G GRCh38
NC_000005.9:g.225454C>G , CM000667.1:g.225454C>G GRCh37
NC_000005.8:g.278454C>G NCBI36
NG_012339.1:g.12099C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264932.11:c.313-80C>G MANE Select ENSP00000264932.6:n.313-80C>G
ENST00000651543.1:c.313-80C>G ENSP00000499215.1:n.313-80C>G
ENST00000264932.10:c.313-80C>G ENSP00000264932.6:n.313-80C>G
ENST00000504309.5:c.313-80C>G ENSP00000426514.1:n.313-80C>G
ENST00000504824.5:n.298-80C>G
ENST00000505555.5:n.353-80C>G
ENST00000509632.5:c.*141-80C>G ENSP00000425077.1:n.*141-80C>G
ENST00000510361.5:c.313-544C>G ENSP00000427703.1:n.313-544C>G
ENST00000617470.4:c.313-80C>G ENSP00000484230.1:n.313-80C>G
NM_001294332.1:c.313-544C>G NP_001281261.1:n.313-544C>G
NM_004168.3:c.313-80C>G NP_004159.2:n.313-80C>G
XM_005248331.2:c.313-80C>G XP_005248388.1:n.313-80C>G
XM_011514072.1:c.313-80C>G XP_011512374.1:n.313-80C>G
XM_011514073.1:c.313-80C>G XP_011512375.1:n.313-80C>G
XR_925638.1:n.446-80C>G
NM_001330758.1:c.313-80C>G NP_001317687.1:n.313-80C>G
XM_011514072.2:c.313-80C>G XP_011512374.1:n.313-80C>G
XM_011514073.2:c.313-80C>G XP_011512375.1:n.313-80C>G
XM_017009685.2:c.313-80C>G XP_016865174.1:n.313-80C>G
XM_024446143.1:c.313-544C>G XP_024301911.1:n.313-544C>G
XR_002956167.1:n.360-80C>G
NM_004168.4:c.313-80C>G MANE Select NP_004159.2:n.313-80C>G
NM_001294332.2:c.313-544C>G NP_001281261.1:n.313-544C>G
NM_001330758.2:c.313-80C>G NP_001317687.1:n.313-80C>G