Canonical Allele Identifier: CA155150

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.256357G>A , CM000667.2:g.256357G>A	GRCh38
NC_000005.9:g.256472G>A , CM000667.1:g.256472G>A	GRCh37
NC_000005.8:g.309472G>A	NCBI36
NG_012339.1:g.43117G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1932G>A MANE Select	ENSP00000264932.6:p.Val644=
ENST00000651543.1:c.*665G>A	ENSP00000499215.1:n.*665G>A
ENST00000264932.10:c.1932G>A	ENSP00000264932.6:p.Val644=
ENST00000503674.5:n.2104G>A
ENST00000504309.5:c.1689G>A	ENSP00000426514.1:p.Val563=
ENST00000507522.1:n.322G>A
ENST00000509082.1:n.109G>A
ENST00000509564.1:c.305G>A	ENSP00000421911.1:p.Ter102=
ENST00000510361.5:c.1788G>A	ENSP00000427703.1:p.Val596=
ENST00000511810.5:n.2679G>A
ENST00000514027.5:n.1887G>A
ENST00000515752.5:n.1518G>A
ENST00000515815.5:c.379G>A
ENST00000617470.4:c.1497G>A	ENSP00000484230.1:p.Val499=
NM_001294332.1:c.1788G>A	NP_001281261.1:p.Val596=
NM_004168.3:c.1932G>A	NP_004159.2:p.Val644=
XM_005248331.2:c.1689G>A	XP_005248388.1:p.Val563=
XM_011514072.1:c.1908+1851G>A	XP_011512374.1:n.1908+1851G>A
XM_011514073.1:c.1665+1851G>A	XP_011512375.1:n.1665+1851G>A
XR_925638.1:n.2041+1851G>A
NM_001330758.1:c.1689G>A	NP_001317687.1:p.Val563=
XM_011514072.2:c.1908+1851G>A	XP_011512374.1:n.1908+1851G>A
XM_011514073.2:c.1665+1851G>A	XP_011512375.1:n.1665+1851G>A
XM_017009685.2:c.*1401G>A	XP_016865174.1:n.*1401G>A
XM_024446143.1:c.*1401G>A	XP_024301911.1:n.*1401G>A
XR_002956167.1:n.4903G>A
NM_004168.4:c.1932G>A MANE Select	NP_004159.2:p.Val644=
NM_001294332.2:c.1788G>A	NP_001281261.1:p.Val596=
NM_001330758.2:c.1689G>A	NP_001317687.1:p.Val563=