Canonical Allele Identifier: CA359013997

Gene: SDHA

Linked Data

• MyVariant Identifiers: chr5:g.236640G>T (hg19) ; chr5:g.236525G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236525G>T , CM000667.2:g.236525G>T	GRCh38
NC_000005.9:g.236640G>T , CM000667.1:g.236640G>T	GRCh37
NC_000005.8:g.289640G>T	NCBI36
NG_012339.1:g.23285G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1358G>T MANE Select	ENSP00000264932.6:p.Gly453Val
ENST00000651543.1:c.*91G>T	ENSP00000499215.1:n.*91G>T
ENST00000264932.10:c.1358G>T	ENSP00000264932.6:p.Gly453Val
ENST00000504309.5:c.1358G>T	ENSP00000426514.1:p.Gly453Val
ENST00000505555.5:n.1398G>T
ENST00000510361.5:c.1214G>T	ENSP00000427703.1:p.Gly405Val
ENST00000511810.5:n.2105G>T
ENST00000514027.5:n.1313G>T
ENST00000515752.5:n.944G>T
ENST00000515815.5:c.13G>T
ENST00000617470.4:c.923G>T	ENSP00000484230.1:p.Gly308Val
NM_001294332.1:c.1214G>T	NP_001281261.1:p.Gly405Val
NM_004168.3:c.1358G>T	NP_004159.2:p.Gly453Val
XM_005248331.2:c.1358G>T	XP_005248388.1:p.Gly453Val
XM_011514072.1:c.1358G>T	XP_011512374.1:p.Gly453Val
XM_011514073.1:c.1358G>T	XP_011512375.1:p.Gly453Val
XR_925638.1:n.1491G>T
NM_001330758.1:c.1358G>T	NP_001317687.1:p.Gly453Val
XM_011514072.2:c.1358G>T	XP_011512374.1:p.Gly453Val
XM_011514073.2:c.1358G>T	XP_011512375.1:p.Gly453Val
XM_017009685.2:c.1358G>T	XP_016865174.1:p.Gly453Val
XM_024446143.1:c.1214G>T	XP_024301911.1:p.Gly405Val
XR_002956167.1:n.1405G>T
NM_004168.4:c.1358G>T MANE Select	NP_004159.2:p.Gly453Val
NM_001294332.2:c.1214G>T	NP_001281261.1:p.Gly405Val
NM_001330758.2:c.1358G>T	NP_001317687.1:p.Gly453Val