Canonical Allele Identifier: CA1521984390

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.225903G= , CM000667.2:g.225903G=	GRCh38
NC_000005.9:g.226018G= , CM000667.1:g.226018G=	GRCh37
NC_000005.8:g.279018G=	NCBI36
NG_012339.1:g.12663G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.477G= MANE Select	ENSP00000264932.6:p.Pro159=
ENST00000651543.1:c.477G=	ENSP00000499215.1:p.Pro159=
ENST00000264932.10:c.477G=	ENSP00000264932.6:p.Pro159=
ENST00000504309.5:c.477G=	ENSP00000426514.1:p.Pro159=
ENST00000504824.5:n.462G=
ENST00000505555.5:n.517G=
ENST00000509420.5:n.271G=
ENST00000510361.5:c.333G=	ENSP00000427703.1:p.Pro111=
ENST00000617470.4:c.380+417G=	ENSP00000484230.1:n.380+417G=
NM_001294332.1:c.333G=	NP_001281261.1:p.Pro111=
NM_004168.3:c.477G=	NP_004159.2:p.Pro159=
XM_005248331.2:c.477G=	XP_005248388.1:p.Pro159=
XM_011514072.1:c.477G=	XP_011512374.1:p.Pro159=
XM_011514073.1:c.477G=	XP_011512375.1:p.Pro159=
XR_925638.1:n.610G=
NM_001330758.1:c.477G=	NP_001317687.1:p.Pro159=
XM_011514072.2:c.477G=	XP_011512374.1:p.Pro159=
XM_011514073.2:c.477G=	XP_011512375.1:p.Pro159=
XM_017009685.2:c.477G=	XP_016865174.1:p.Pro159=
XM_024446143.1:c.333G=	XP_024301911.1:p.Pro111=
XR_002956167.1:n.524G=
NM_004168.4:c.477G= MANE Select	NP_004159.2:p.Pro159=
NM_001294332.2:c.333G=	NP_001281261.1:p.Pro111=
NM_001330758.2:c.477G=	NP_001317687.1:p.Pro159=