Canonical Allele Identifier: CA1521983064

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.225350G= , CM000667.2:g.225350G=	GRCh38
NC_000005.9:g.225465G= , CM000667.1:g.225465G=	GRCh37
NC_000005.8:g.278465G=	NCBI36
NG_012339.1:g.12110G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.313-69G= MANE Select	ENSP00000264932.6:n.313-69G=
ENST00000651543.1:c.313-69G=	ENSP00000499215.1:n.313-69G=
ENST00000264932.10:c.313-69G=	ENSP00000264932.6:n.313-69G=
ENST00000504309.5:c.313-69G=	ENSP00000426514.1:n.313-69G=
ENST00000504824.5:n.298-69G=
ENST00000505555.5:n.353-69G=
ENST00000509632.5:c.*141-69G=	ENSP00000425077.1:n.*141-69G=
ENST00000510361.5:c.313-533G=	ENSP00000427703.1:n.313-533G=
ENST00000617470.4:c.313-69G=	ENSP00000484230.1:n.313-69G=
NM_001294332.1:c.313-533G=	NP_001281261.1:n.313-533G=
NM_004168.3:c.313-69G=	NP_004159.2:n.313-69G=
XM_005248331.2:c.313-69G=	XP_005248388.1:n.313-69G=
XM_011514072.1:c.313-69G=	XP_011512374.1:n.313-69G=
XM_011514073.1:c.313-69G=	XP_011512375.1:n.313-69G=
XR_925638.1:n.446-69G=
NM_001330758.1:c.313-69G=	NP_001317687.1:n.313-69G=
XM_011514072.2:c.313-69G=	XP_011512374.1:n.313-69G=
XM_011514073.2:c.313-69G=	XP_011512375.1:n.313-69G=
XM_017009685.2:c.313-69G=	XP_016865174.1:n.313-69G=
XM_024446143.1:c.313-533G=	XP_024301911.1:n.313-533G=
XR_002956167.1:n.360-69G=
NM_004168.4:c.313-69G= MANE Select	NP_004159.2:n.313-69G=
NM_001294332.2:c.313-533G=	NP_001281261.1:n.313-533G=
NM_001330758.2:c.313-69G=	NP_001317687.1:n.313-69G=