Canonical Allele Identifier: CA3173478

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.256402A>G , CM000667.2:g.256402A>G	GRCh38
NC_000005.9:g.256517A>G , CM000667.1:g.256517A>G	GRCh37
NC_000005.8:g.309517A>G	NCBI36
NG_012339.1:g.43162A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004168.4:c.1977A>G MANE Select	NP_004159.2:p.Pro659=
ENST00000264932.11:c.1977A>G MANE Select	ENSP00000264932.6:p.Pro659=
NM_001294332.1:c.1833A>G	NP_001281261.1:p.Pro611=
NM_001294332.2:c.1833A>G	NP_001281261.1:p.Pro611=
NM_001330758.1:c.1734A>G	NP_001317687.1:p.Pro578=
NM_001330758.2:c.1734A>G	NP_001317687.1:p.Pro578=
NM_004168.3:c.1977A>G	NP_004159.2:p.Pro659=
ENST00000264932.10:c.1977A>G	ENSP00000264932.6:p.Pro659=
ENST00000503674.5:n.2149A>G
ENST00000504309.5:c.1734A>G	ENSP00000426514.1:p.Pro578=
ENST00000507522.1:n.367A>G
ENST00000509082.1:n.154A>G
ENST00000509564.1:c.350A>G	ENSP00000421911.1:n.350A>G
ENST00000510361.5:c.1833A>G	ENSP00000427703.1:p.Pro611=
ENST00000511810.5:n.2724A>G
ENST00000514027.5:n.1932A>G
ENST00000515752.5:n.1563A>G
ENST00000515815.5:c.424A>G
ENST00000617470.4:c.1542A>G	ENSP00000484230.1:p.Pro514=
ENST00000651543.1:c.*710A>G	ENSP00000499215.1:n.*710A>G
XM_005248331.2:c.1734A>G	XP_005248388.1:p.Pro578=
XM_011514072.1:c.1908+1896A>G	XP_011512374.1:n.1908+1896A>G
XM_011514072.2:c.1908+1896A>G	XP_011512374.1:n.1908+1896A>G
XM_011514073.1:c.1665+1896A>G	XP_011512375.1:n.1665+1896A>G
XM_011514073.2:c.1665+1896A>G	XP_011512375.1:n.1665+1896A>G
XM_017009685.2:c.*1446A>G	XP_016865174.1:n.*1446A>G
XM_024446143.1:c.*1446A>G	XP_024301911.1:n.*1446A>G
XR_002956167.1:n.4948A>G
XR_925638.1:n.2041+1896A>G