Canonical Allele Identifier: CA359013954

Gene: SDHA

Linked Data

• ClinVar Variation Id: 1954001
• ClinVar RCV Id: RCV002705297
• dbSNP Id: rs2126589937
• MyVariant Identifiers: chr5:g.236618G>A (hg19) ; chr5:g.236503G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236503G>A , CM000667.2:g.236503G>A	GRCh38
NC_000005.9:g.236618G>A , CM000667.1:g.236618G>A	GRCh37
NC_000005.8:g.289618G>A	NCBI36
NG_012339.1:g.23263G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1336G>A MANE Select	ENSP00000264932.6:p.Val446Ile
ENST00000651543.1:c.*69G>A	ENSP00000499215.1:n.*69G>A
ENST00000264932.10:c.1336G>A	ENSP00000264932.6:p.Val446Ile
ENST00000504309.5:c.1336G>A	ENSP00000426514.1:p.Val446Ile
ENST00000505555.5:n.1376G>A
ENST00000510361.5:c.1192G>A	ENSP00000427703.1:p.Val398Ile
ENST00000511810.5:n.2083G>A
ENST00000512962.5:n.922G>A
ENST00000514027.5:n.1291G>A
ENST00000515752.5:n.922G>A
ENST00000617470.4:c.901G>A	ENSP00000484230.1:p.Val301Ile
NM_001294332.1:c.1192G>A	NP_001281261.1:p.Val398Ile
NM_004168.3:c.1336G>A	NP_004159.2:p.Val446Ile
XM_005248331.2:c.1336G>A	XP_005248388.1:p.Val446Ile
XM_011514072.1:c.1336G>A	XP_011512374.1:p.Val446Ile
XM_011514073.1:c.1336G>A	XP_011512375.1:p.Val446Ile
XR_925638.1:n.1469G>A
NM_001330758.1:c.1336G>A	NP_001317687.1:p.Val446Ile
XM_011514072.2:c.1336G>A	XP_011512374.1:p.Val446Ile
XM_011514073.2:c.1336G>A	XP_011512375.1:p.Val446Ile
XM_017009685.2:c.1336G>A	XP_016865174.1:p.Val446Ile
XM_024446143.1:c.1192G>A	XP_024301911.1:p.Val398Ile
XR_002956167.1:n.1383G>A
NM_004168.4:c.1336G>A MANE Select	NP_004159.2:p.Val446Ile
NM_001294332.2:c.1192G>A	NP_001281261.1:p.Val398Ile
NM_001330758.2:c.1336G>A	NP_001317687.1:p.Val446Ile