Canonical Allele Identifier: CA359014125

Gene: SDHA

Linked Data

• MyVariant Identifiers: chr5:g.236705T>A (hg19) ; chr5:g.236590T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236590T>A , CM000667.2:g.236590T>A	GRCh38
NC_000005.9:g.236705T>A , CM000667.1:g.236705T>A	GRCh37
NC_000005.8:g.289705T>A	NCBI36
NG_012339.1:g.23350T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1423T>A MANE Select	ENSP00000264932.6:p.Cys475Ser
ENST00000651543.1:c.*156T>A	ENSP00000499215.1:n.*156T>A
ENST00000264932.10:c.1423T>A	ENSP00000264932.6:p.Cys475Ser
ENST00000504309.5:c.1423T>A	ENSP00000426514.1:p.Cys475Ser
ENST00000505555.5:n.1463T>A
ENST00000510361.5:c.1279T>A	ENSP00000427703.1:p.Cys427Ser
ENST00000511810.5:n.2170T>A
ENST00000514027.5:n.1378T>A
ENST00000515752.5:n.1009T>A
ENST00000515815.5:c.78T>A
ENST00000617470.4:c.988T>A	ENSP00000484230.1:p.Cys330Ser
NM_001294332.1:c.1279T>A	NP_001281261.1:p.Cys427Ser
NM_004168.3:c.1423T>A	NP_004159.2:p.Cys475Ser
XM_005248331.2:c.1423T>A	XP_005248388.1:p.Cys475Ser
XM_011514072.1:c.1423T>A	XP_011512374.1:p.Cys475Ser
XM_011514073.1:c.1423T>A	XP_011512375.1:p.Cys475Ser
XR_925638.1:n.1556T>A
NM_001330758.1:c.1423T>A	NP_001317687.1:p.Cys475Ser
XM_011514072.2:c.1423T>A	XP_011512374.1:p.Cys475Ser
XM_011514073.2:c.1423T>A	XP_011512375.1:p.Cys475Ser
XM_017009685.2:c.1423T>A	XP_016865174.1:p.Cys475Ser
XM_024446143.1:c.1279T>A	XP_024301911.1:p.Cys427Ser
XR_002956167.1:n.1470T>A
NM_004168.4:c.1423T>A MANE Select	NP_004159.2:p.Cys475Ser
NM_001294332.2:c.1279T>A	NP_001281261.1:p.Cys427Ser
NM_001330758.2:c.1423T>A	NP_001317687.1:p.Cys475Ser