Canonical Allele Identifier: CA442692095

Gene: SDHA

Linked Data

• MyVariant Identifiers: chr5:g.236608C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.236493C>G , CM000667.2:g.236493C>G	GRCh38
NC_000005.9:g.236608C>G , CM000667.1:g.236608C>G	GRCh37
NC_000005.8:g.289608C>G	NCBI36
NG_012339.1:g.23253C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264932.11:c.1326C>G MANE Select	ENSP00000264932.6:p.Ala442=
ENST00000651543.1:c.*59C>G	ENSP00000499215.1:n.*59C>G
ENST00000264932.10:c.1326C>G	ENSP00000264932.6:p.Ala442=
ENST00000504309.5:c.1326C>G	ENSP00000426514.1:p.Ala442=
ENST00000505555.5:n.1366C>G
ENST00000510361.5:c.1182C>G	ENSP00000427703.1:p.Ala394=
ENST00000511810.5:n.2073C>G
ENST00000512962.5:n.912C>G
ENST00000514027.5:n.1281C>G
ENST00000515752.5:n.912C>G
ENST00000617470.4:c.891C>G	ENSP00000484230.1:p.Ala297=
NM_001294332.1:c.1182C>G	NP_001281261.1:p.Ala394=
NM_004168.3:c.1326C>G	NP_004159.2:p.Ala442=
XM_005248331.2:c.1326C>G	XP_005248388.1:p.Ala442=
XM_011514072.1:c.1326C>G	XP_011512374.1:p.Ala442=
XM_011514073.1:c.1326C>G	XP_011512375.1:p.Ala442=
XR_925638.1:n.1459C>G
NM_001330758.1:c.1326C>G	NP_001317687.1:p.Ala442=
XM_011514072.2:c.1326C>G	XP_011512374.1:p.Ala442=
XM_011514073.2:c.1326C>G	XP_011512375.1:p.Ala442=
XM_017009685.2:c.1326C>G	XP_016865174.1:p.Ala442=
XM_024446143.1:c.1182C>G	XP_024301911.1:p.Ala394=
XR_002956167.1:n.1373C>G
NM_004168.4:c.1326C>G MANE Select	NP_004159.2:p.Ala442=
NM_001294332.2:c.1182C>G	NP_001281261.1:p.Ala394=
NM_001330758.2:c.1326C>G	NP_001317687.1:p.Ala442=