Canonical Allele Identifier: CA1521981678

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.224432C= , CM000667.2:g.224432C=	GRCh38
NC_000005.9:g.224547C= , CM000667.1:g.224547C=	GRCh37
NC_000005.8:g.277547C=	NCBI36
NG_012339.1:g.11192C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004168.4:c.223C= MANE Select	NP_004159.2:p.Arg75=
ENST00000264932.11:c.223C= MANE Select	ENSP00000264932.6:p.Arg75=
NM_001294332.1:c.223C=	NP_001281261.1:p.Arg75=
NM_001294332.2:c.223C=	NP_001281261.1:p.Arg75=
NM_001330758.1:c.223C=	NP_001317687.1:p.Arg75=
NM_001330758.2:c.223C=	NP_001317687.1:p.Arg75=
NM_004168.3:c.223C=	NP_004159.2:p.Arg75=
ENST00000264932.10:c.223C=	ENSP00000264932.6:p.Arg75=
ENST00000502379.5:n.268C=
ENST00000504309.5:c.223C=	ENSP00000426514.1:p.Arg75=
ENST00000504824.5:n.208C=
ENST00000505555.5:n.263C=
ENST00000509632.5:c.*51C=	ENSP00000425077.1:n.*51C=
ENST00000510361.5:c.223C=	ENSP00000427703.1:p.Arg75=
ENST00000617470.4:c.223C=	ENSP00000484230.1:p.Arg75=
ENST00000651543.1:c.223C=	ENSP00000499215.1:p.Arg75=
XM_005248331.2:c.223C=	XP_005248388.1:p.Arg75=
XM_011514072.1:c.223C=	XP_011512374.1:p.Arg75=
XM_011514072.2:c.223C=	XP_011512374.1:p.Arg75=
XM_011514073.1:c.223C=	XP_011512375.1:p.Arg75=
XM_011514073.2:c.223C=	XP_011512375.1:p.Arg75=
XM_017009685.2:c.223C=	XP_016865174.1:p.Arg75=
XM_024446143.1:c.223C=	XP_024301911.1:p.Arg75=
XR_002956167.1:n.270C=
XR_925638.1:n.356C=