Canonical Allele Identifier: CA359013999

Gene: SDHA

Linked Data

• ClinVar Variation Id: 581048
• ClinVar RCV Id: RCV000704760
• dbSNP Id: rs1057517550
• MyVariant Identifiers: chr5:g.236642G>T (hg19) ; chr5:g.236527G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236527G>T , CM000667.2:g.236527G>T	GRCh38
NC_000005.9:g.236642G>T , CM000667.1:g.236642G>T	GRCh37
NC_000005.8:g.289642G>T	NCBI36
NG_012339.1:g.23287G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1360G>T MANE Select	ENSP00000264932.6:p.Ala454Ser
ENST00000651543.1:c.*93G>T	ENSP00000499215.1:n.*93G>T
ENST00000264932.10:c.1360G>T	ENSP00000264932.6:p.Ala454Ser
ENST00000504309.5:c.1360G>T	ENSP00000426514.1:p.Ala454Ser
ENST00000505555.5:n.1400G>T
ENST00000510361.5:c.1216G>T	ENSP00000427703.1:p.Ala406Ser
ENST00000511810.5:n.2107G>T
ENST00000514027.5:n.1315G>T
ENST00000515752.5:n.946G>T
ENST00000515815.5:c.15G>T
ENST00000617470.4:c.925G>T	ENSP00000484230.1:p.Ala309Ser
NM_001294332.1:c.1216G>T	NP_001281261.1:p.Ala406Ser
NM_004168.3:c.1360G>T	NP_004159.2:p.Ala454Ser
XM_005248331.2:c.1360G>T	XP_005248388.1:p.Ala454Ser
XM_011514072.1:c.1360G>T	XP_011512374.1:p.Ala454Ser
XM_011514073.1:c.1360G>T	XP_011512375.1:p.Ala454Ser
XR_925638.1:n.1493G>T
NM_001330758.1:c.1360G>T	NP_001317687.1:p.Ala454Ser
XM_011514072.2:c.1360G>T	XP_011512374.1:p.Ala454Ser
XM_011514073.2:c.1360G>T	XP_011512375.1:p.Ala454Ser
XM_017009685.2:c.1360G>T	XP_016865174.1:p.Ala454Ser
XM_024446143.1:c.1216G>T	XP_024301911.1:p.Ala406Ser
XR_002956167.1:n.1407G>T
NM_004168.4:c.1360G>T MANE Select	NP_004159.2:p.Ala454Ser
NM_001294332.2:c.1216G>T	NP_001281261.1:p.Ala406Ser
NM_001330758.2:c.1360G>T	NP_001317687.1:p.Ala454Ser