Canonical Allele Identifier: CA3172834

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.225582G>C , CM000667.2:g.225582G>C	GRCh38
NC_000005.9:g.225697G>C , CM000667.1:g.225697G>C	GRCh37
NC_000005.8:g.278697G>C	NCBI36
NG_012339.1:g.12342G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.456+20G>C MANE Select	ENSP00000264932.6:n.456+20G>C
ENST00000651543.1:c.456+20G>C	ENSP00000499215.1:n.456+20G>C
ENST00000264932.10:c.456+20G>C	ENSP00000264932.6:n.456+20G>C
ENST00000504309.5:c.456+20G>C	ENSP00000426514.1:n.456+20G>C
ENST00000504824.5:n.441+20G>C
ENST00000505555.5:n.496+20G>C
ENST00000510361.5:c.313-301G>C	ENSP00000427703.1:n.313-301G>C
ENST00000617470.4:c.380+96G>C	ENSP00000484230.1:n.380+96G>C
NM_001294332.1:c.313-301G>C	NP_001281261.1:n.313-301G>C
NM_004168.3:c.456+20G>C	NP_004159.2:n.456+20G>C
XM_005248331.2:c.456+20G>C	XP_005248388.1:n.456+20G>C
XM_011514072.1:c.456+20G>C	XP_011512374.1:n.456+20G>C
XM_011514073.1:c.456+20G>C	XP_011512375.1:n.456+20G>C
XR_925638.1:n.589+20G>C
NM_001330758.1:c.456+20G>C	NP_001317687.1:n.456+20G>C
XM_011514072.2:c.456+20G>C	XP_011512374.1:n.456+20G>C
XM_011514073.2:c.456+20G>C	XP_011512375.1:n.456+20G>C
XM_017009685.2:c.456+20G>C	XP_016865174.1:n.456+20G>C
XM_024446143.1:c.313-301G>C	XP_024301911.1:n.313-301G>C
XR_002956167.1:n.503+20G>C
NM_004168.4:c.456+20G>C MANE Select	NP_004159.2:n.456+20G>C
NM_001294332.2:c.313-301G>C	NP_001281261.1:n.313-301G>C
NM_001330758.2:c.456+20G>C	NP_001317687.1:n.456+20G>C