Canonical Allele Identifier: CA359014052

Gene: SDHA

Linked Data

• MyVariant Identifiers: chr5:g.236669T>G (hg19) ; chr5:g.236554T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236554T>G , CM000667.2:g.236554T>G	GRCh38
NC_000005.9:g.236669T>G , CM000667.1:g.236669T>G	GRCh37
NC_000005.8:g.289669T>G	NCBI36
NG_012339.1:g.23314T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1387T>G MANE Select	ENSP00000264932.6:p.Phe463Val
ENST00000651543.1:c.*120T>G	ENSP00000499215.1:n.*120T>G
ENST00000264932.10:c.1387T>G	ENSP00000264932.6:p.Phe463Val
ENST00000504309.5:c.1387T>G	ENSP00000426514.1:p.Phe463Val
ENST00000505555.5:n.1427T>G
ENST00000510361.5:c.1243T>G	ENSP00000427703.1:p.Phe415Val
ENST00000511810.5:n.2134T>G
ENST00000514027.5:n.1342T>G
ENST00000515752.5:n.973T>G
ENST00000515815.5:c.42T>G
ENST00000617470.4:c.952T>G	ENSP00000484230.1:p.Phe318Val
NM_001294332.1:c.1243T>G	NP_001281261.1:p.Phe415Val
NM_004168.3:c.1387T>G	NP_004159.2:p.Phe463Val
XM_005248331.2:c.1387T>G	XP_005248388.1:p.Phe463Val
XM_011514072.1:c.1387T>G	XP_011512374.1:p.Phe463Val
XM_011514073.1:c.1387T>G	XP_011512375.1:p.Phe463Val
XR_925638.1:n.1520T>G
NM_001330758.1:c.1387T>G	NP_001317687.1:p.Phe463Val
XM_011514072.2:c.1387T>G	XP_011512374.1:p.Phe463Val
XM_011514073.2:c.1387T>G	XP_011512375.1:p.Phe463Val
XM_017009685.2:c.1387T>G	XP_016865174.1:p.Phe463Val
XM_024446143.1:c.1243T>G	XP_024301911.1:p.Phe415Val
XR_002956167.1:n.1434T>G
NM_004168.4:c.1387T>G MANE Select	NP_004159.2:p.Phe463Val
NM_001294332.2:c.1243T>G	NP_001281261.1:p.Phe415Val
NM_001330758.2:c.1387T>G	NP_001317687.1:p.Phe463Val