Canonical Allele Identifier: CA155160

Gene: SDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.230996T>C , CM000667.2:g.230996T>C	GRCh38
NC_000005.9:g.231111T>C , CM000667.1:g.231111T>C	GRCh37
NC_000005.8:g.284111T>C	NCBI36
NG_012339.1:g.17756T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.891T>C MANE Select	ENSP00000264932.6:p.Pro297=
ENST00000651543.1:c.891T>C	ENSP00000499215.1:p.Pro297=
ENST00000264932.10:c.891T>C	ENSP00000264932.6:p.Pro297=
ENST00000504309.5:c.891T>C	ENSP00000426514.1:p.Pro297=
ENST00000504824.5:n.876T>C
ENST00000505555.5:n.931T>C
ENST00000510361.5:c.747T>C	ENSP00000427703.1:p.Pro249=
ENST00000512962.5:n.54T>C
ENST00000514027.5:n.846T>C
ENST00000514233.1:n.401T>C
ENST00000515752.5:n.54T>C
ENST00000617470.4:c.456T>C	ENSP00000484230.1:p.Pro152=
NM_001294332.1:c.747T>C	NP_001281261.1:p.Pro249=
NM_004168.3:c.891T>C	NP_004159.2:p.Pro297=
XM_005248331.2:c.891T>C	XP_005248388.1:p.Pro297=
XM_011514072.1:c.891T>C	XP_011512374.1:p.Pro297=
XM_011514073.1:c.891T>C	XP_011512375.1:p.Pro297=
XR_925638.1:n.1024T>C
NM_001330758.1:c.891T>C	NP_001317687.1:p.Pro297=
XM_011514072.2:c.891T>C	XP_011512374.1:p.Pro297=
XM_011514073.2:c.891T>C	XP_011512375.1:p.Pro297=
XM_017009685.2:c.891T>C	XP_016865174.1:p.Pro297=
XM_024446143.1:c.747T>C	XP_024301911.1:p.Pro249=
XR_002956167.1:n.938T>C
NM_004168.4:c.891T>C MANE Select	NP_004159.2:p.Pro297=
NM_001294332.2:c.747T>C	NP_001281261.1:p.Pro249=
NM_001330758.2:c.891T>C	NP_001317687.1:p.Pro297=