Canonical Allele Identifier: CA359009847

Gene: SDHA

Linked Data

• ClinVar Variation Id: 857526
• ClinVar RCV Id: RCV001063216
• dbSNP Id: rs989318548
• MyVariant Identifiers: chr5:g.226009T>G (hg19) ; chr5:g.225894T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.225894T>G , CM000667.2:g.225894T>G	GRCh38
NC_000005.9:g.226009T>G , CM000667.1:g.226009T>G	GRCh37
NC_000005.8:g.279009T>G	NCBI36
NG_012339.1:g.12654T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.468T>G MANE Select	ENSP00000264932.6:p.Tyr156Ter
ENST00000651543.1:c.468T>G	ENSP00000499215.1:p.Tyr156Ter
ENST00000264932.10:c.468T>G	ENSP00000264932.6:p.Tyr156Ter
ENST00000504309.5:c.468T>G	ENSP00000426514.1:p.Tyr156Ter
ENST00000504824.5:n.453T>G
ENST00000505555.5:n.508T>G
ENST00000509420.5:n.262T>G
ENST00000510361.5:c.324T>G	ENSP00000427703.1:p.Tyr108Ter
ENST00000617470.4:c.380+408T>G	ENSP00000484230.1:n.380+408T>G
NM_001294332.1:c.324T>G	NP_001281261.1:p.Tyr108Ter
NM_004168.3:c.468T>G	NP_004159.2:p.Tyr156Ter
XM_005248331.2:c.468T>G	XP_005248388.1:p.Tyr156Ter
XM_011514072.1:c.468T>G	XP_011512374.1:p.Tyr156Ter
XM_011514073.1:c.468T>G	XP_011512375.1:p.Tyr156Ter
XR_925638.1:n.601T>G
NM_001330758.1:c.468T>G	NP_001317687.1:p.Tyr156Ter
XM_011514072.2:c.468T>G	XP_011512374.1:p.Tyr156Ter
XM_011514073.2:c.468T>G	XP_011512375.1:p.Tyr156Ter
XM_017009685.2:c.468T>G	XP_016865174.1:p.Tyr156Ter
XM_024446143.1:c.324T>G	XP_024301911.1:p.Tyr108Ter
XR_002956167.1:n.515T>G
NM_004168.4:c.468T>G MANE Select	NP_004159.2:p.Tyr156Ter
NM_001294332.2:c.324T>G	NP_001281261.1:p.Tyr108Ter
NM_001330758.2:c.468T>G	NP_001317687.1:p.Tyr156Ter