Canonical Allele Identifier: CA1521984325

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.225892T= , CM000667.2:g.225892T=	GRCh38
NC_000005.9:g.226007T= , CM000667.1:g.226007T=	GRCh37
NC_000005.8:g.279007T=	NCBI36
NG_012339.1:g.12652T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.466T= MANE Select	ENSP00000264932.6:p.Tyr156=
ENST00000651543.1:c.466T=	ENSP00000499215.1:p.Tyr156=
ENST00000264932.10:c.466T=	ENSP00000264932.6:p.Tyr156=
ENST00000504309.5:c.466T=	ENSP00000426514.1:p.Tyr156=
ENST00000504824.5:n.451T=
ENST00000505555.5:n.506T=
ENST00000509420.5:n.260T=
ENST00000510361.5:c.322T=	ENSP00000427703.1:p.Tyr108=
ENST00000617470.4:c.380+406T=	ENSP00000484230.1:n.380+406T=
NM_001294332.1:c.322T=	NP_001281261.1:p.Tyr108=
NM_004168.3:c.466T=	NP_004159.2:p.Tyr156=
XM_005248331.2:c.466T=	XP_005248388.1:p.Tyr156=
XM_011514072.1:c.466T=	XP_011512374.1:p.Tyr156=
XM_011514073.1:c.466T=	XP_011512375.1:p.Tyr156=
XR_925638.1:n.599T=
NM_001330758.1:c.466T=	NP_001317687.1:p.Tyr156=
XM_011514072.2:c.466T=	XP_011512374.1:p.Tyr156=
XM_011514073.2:c.466T=	XP_011512375.1:p.Tyr156=
XM_017009685.2:c.466T=	XP_016865174.1:p.Tyr156=
XM_024446143.1:c.322T=	XP_024301911.1:p.Tyr108=
XR_002956167.1:n.513T=
NM_004168.4:c.466T= MANE Select	NP_004159.2:p.Tyr156=
NM_001294332.2:c.322T=	NP_001281261.1:p.Tyr108=
NM_001330758.2:c.466T=	NP_001317687.1:p.Tyr156=