Canonical Allele Identifier: CA16611864

Gene: SDHA

Linked Data

• ClinVar Variation Id: 412354
• ClinVar RCV Id: RCV000458845
• dbSNP Id: rs1060503710
• gnomAD v3: 5-225411-G-A
• gnomAD v4: 5-225411-G-A
• MyVariant Identifiers: chr5:g.225526G>A (hg19) ; chr5:g.225411G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.225411G>A , CM000667.2:g.225411G>A	GRCh38
NC_000005.9:g.225526G>A , CM000667.1:g.225526G>A	GRCh37
NC_000005.8:g.278526G>A	NCBI36
NG_012339.1:g.12171G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.313-8G>A MANE Select	ENSP00000264932.6:n.313-8G>A
ENST00000651543.1:c.313-8G>A	ENSP00000499215.1:n.313-8G>A
ENST00000264932.10:c.313-8G>A	ENSP00000264932.6:n.313-8G>A
ENST00000504309.5:c.313-8G>A	ENSP00000426514.1:n.313-8G>A
ENST00000504824.5:n.298-8G>A
ENST00000505555.5:n.353-8G>A
ENST00000509632.5:c.*141-8G>A	ENSP00000425077.1:n.*141-8G>A
ENST00000510361.5:c.313-472G>A	ENSP00000427703.1:n.313-472G>A
ENST00000617470.4:c.313-8G>A	ENSP00000484230.1:n.313-8G>A
NM_001294332.1:c.313-472G>A	NP_001281261.1:n.313-472G>A
NM_004168.3:c.313-8G>A	NP_004159.2:n.313-8G>A
XM_005248331.2:c.313-8G>A	XP_005248388.1:n.313-8G>A
XM_011514072.1:c.313-8G>A	XP_011512374.1:n.313-8G>A
XM_011514073.1:c.313-8G>A	XP_011512375.1:n.313-8G>A
XR_925638.1:n.446-8G>A
NM_001330758.1:c.313-8G>A	NP_001317687.1:n.313-8G>A
XM_011514072.2:c.313-8G>A	XP_011512374.1:n.313-8G>A
XM_011514073.2:c.313-8G>A	XP_011512375.1:n.313-8G>A
XM_017009685.2:c.313-8G>A	XP_016865174.1:n.313-8G>A
XM_024446143.1:c.313-472G>A	XP_024301911.1:n.313-472G>A
XR_002956167.1:n.360-8G>A
NM_004168.4:c.313-8G>A MANE Select	NP_004159.2:n.313-8G>A
NM_001294332.2:c.313-472G>A	NP_001281261.1:n.313-472G>A
NM_001330758.2:c.313-8G>A	NP_001317687.1:n.313-8G>A