Canonical Allele Identifier: CA1521983561

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236565A= , CM000667.2:g.236565A=	GRCh38
NC_000005.9:g.236680A= , CM000667.1:g.236680A=	GRCh37
NC_000005.8:g.289680A=	NCBI36
NG_012339.1:g.23325A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1398A= MANE Select	ENSP00000264932.6:p.Ala466=
ENST00000651543.1:c.*131A=	ENSP00000499215.1:n.*131A=
ENST00000264932.10:c.1398A=	ENSP00000264932.6:p.Ala466=
ENST00000504309.5:c.1398A=	ENSP00000426514.1:p.Ala466=
ENST00000505555.5:n.1438A=
ENST00000510361.5:c.1254A=	ENSP00000427703.1:p.Ala418=
ENST00000511810.5:n.2145A=
ENST00000514027.5:n.1353A=
ENST00000515752.5:n.984A=
ENST00000515815.5:c.53A=
ENST00000617470.4:c.963A=	ENSP00000484230.1:p.Ala321=
NM_001294332.1:c.1254A=	NP_001281261.1:p.Ala418=
NM_004168.3:c.1398A=	NP_004159.2:p.Ala466=
XM_005248331.2:c.1398A=	XP_005248388.1:p.Ala466=
XM_011514072.1:c.1398A=	XP_011512374.1:p.Ala466=
XM_011514073.1:c.1398A=	XP_011512375.1:p.Ala466=
XR_925638.1:n.1531A=
NM_001330758.1:c.1398A=	NP_001317687.1:p.Ala466=
XM_011514072.2:c.1398A=	XP_011512374.1:p.Ala466=
XM_011514073.2:c.1398A=	XP_011512375.1:p.Ala466=
XM_017009685.2:c.1398A=	XP_016865174.1:p.Ala466=
XM_024446143.1:c.1254A=	XP_024301911.1:p.Ala418=
XR_002956167.1:n.1445A=
NM_004168.4:c.1398A= MANE Select	NP_004159.2:p.Ala466=
NM_001294332.2:c.1254A=	NP_001281261.1:p.Ala418=
NM_001330758.2:c.1398A=	NP_001317687.1:p.Ala466=