Canonical Allele Identifier: CA442690960

Gene: SDHA

Linked Data

• MyVariant Identifiers: chr5:g.225551T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.225436T>G , CM000667.2:g.225436T>G	GRCh38
NC_000005.9:g.225551T>G , CM000667.1:g.225551T>G	GRCh37
NC_000005.8:g.278551T>G	NCBI36
NG_012339.1:g.12196T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.330T>G MANE Select	ENSP00000264932.6:p.Ala110=
ENST00000651543.1:c.330T>G	ENSP00000499215.1:p.Ala110=
ENST00000264932.10:c.330T>G	ENSP00000264932.6:p.Ala110=
ENST00000504309.5:c.330T>G	ENSP00000426514.1:p.Ala110=
ENST00000504824.5:n.315T>G
ENST00000505555.5:n.370T>G
ENST00000509632.5:c.*158T>G	ENSP00000425077.1:n.*158T>G
ENST00000510361.5:c.313-447T>G	ENSP00000427703.1:n.313-447T>G
ENST00000617470.4:c.330T>G	ENSP00000484230.1:p.Ala110=
NM_001294332.1:c.313-447T>G	NP_001281261.1:n.313-447T>G
NM_004168.3:c.330T>G	NP_004159.2:p.Ala110=
XM_005248331.2:c.330T>G	XP_005248388.1:p.Ala110=
XM_011514072.1:c.330T>G	XP_011512374.1:p.Ala110=
XM_011514073.1:c.330T>G	XP_011512375.1:p.Ala110=
XR_925638.1:n.463T>G
NM_001330758.1:c.330T>G	NP_001317687.1:p.Ala110=
XM_011514072.2:c.330T>G	XP_011512374.1:p.Ala110=
XM_011514073.2:c.330T>G	XP_011512375.1:p.Ala110=
XM_017009685.2:c.330T>G	XP_016865174.1:p.Ala110=
XM_024446143.1:c.313-447T>G	XP_024301911.1:n.313-447T>G
XR_002956167.1:n.377T>G
NM_004168.4:c.330T>G MANE Select	NP_004159.2:p.Ala110=
NM_001294332.2:c.313-447T>G	NP_001281261.1:n.313-447T>G
NM_001330758.2:c.330T>G	NP_001317687.1:p.Ala110=