Canonical Allele Identifier: CA1521983326

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236511T= , CM000667.2:g.236511T=	GRCh38
NC_000005.9:g.236626T= , CM000667.1:g.236626T=	GRCh37
NC_000005.8:g.289626T=	NCBI36
NG_012339.1:g.23271T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1344T= MANE Select	ENSP00000264932.6:p.Gly448=
ENST00000651543.1:c.*77T=	ENSP00000499215.1:n.*77T=
ENST00000264932.10:c.1344T=	ENSP00000264932.6:p.Gly448=
ENST00000504309.5:c.1344T=	ENSP00000426514.1:p.Gly448=
ENST00000505555.5:n.1384T=
ENST00000510361.5:c.1200T=	ENSP00000427703.1:p.Gly400=
ENST00000511810.5:n.2091T=
ENST00000512962.5:n.930T=
ENST00000514027.5:n.1299T=
ENST00000515752.5:n.930T=
ENST00000617470.4:c.909T=	ENSP00000484230.1:p.Gly303=
NM_001294332.1:c.1200T=	NP_001281261.1:p.Gly400=
NM_004168.3:c.1344T=	NP_004159.2:p.Gly448=
XM_005248331.2:c.1344T=	XP_005248388.1:p.Gly448=
XM_011514072.1:c.1344T=	XP_011512374.1:p.Gly448=
XM_011514073.1:c.1344T=	XP_011512375.1:p.Gly448=
XR_925638.1:n.1477T=
NM_001330758.1:c.1344T=	NP_001317687.1:p.Gly448=
XM_011514072.2:c.1344T=	XP_011512374.1:p.Gly448=
XM_011514073.2:c.1344T=	XP_011512375.1:p.Gly448=
XM_017009685.2:c.1344T=	XP_016865174.1:p.Gly448=
XM_024446143.1:c.1200T=	XP_024301911.1:p.Gly400=
XR_002956167.1:n.1391T=
NM_004168.4:c.1344T= MANE Select	NP_004159.2:p.Gly448=
NM_001294332.2:c.1200T=	NP_001281261.1:p.Gly400=
NM_001330758.2:c.1344T=	NP_001317687.1:p.Gly448=