Canonical Allele Identifier: CA442692243

Gene: SDHA

Linked Data

• MyVariant Identifiers: chr5:g.240564A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.240449A>C , CM000667.2:g.240449A>C	GRCh38
NC_000005.9:g.240564A>C , CM000667.1:g.240564A>C	GRCh37
NC_000005.8:g.293564A>C	NCBI36
NG_012339.1:g.27209A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264932.11:c.1524A>C MANE Select	ENSP00000264932.6:p.Thr508=
ENST00000651543.1:c.*257A>C	ENSP00000499215.1:n.*257A>C
ENST00000264932.10:c.1524A>C	ENSP00000264932.6:p.Thr508=
ENST00000504309.5:c.1524A>C	ENSP00000426514.1:p.Thr508=
ENST00000505555.5:n.1564A>C
ENST00000509082.1:n.6A>C
ENST00000510361.5:c.1380A>C	ENSP00000427703.1:p.Thr460=
ENST00000511810.5:n.2271A>C
ENST00000514027.5:n.1479A>C
ENST00000515752.5:n.1110A>C
ENST00000515815.5:c.179A>C
ENST00000617470.4:c.1089A>C	ENSP00000484230.1:p.Thr363=
NM_001294332.1:c.1380A>C	NP_001281261.1:p.Thr460=
NM_004168.3:c.1524A>C	NP_004159.2:p.Thr508=
XM_005248331.2:c.1524A>C	XP_005248388.1:p.Thr508=
XM_011514072.1:c.1524A>C	XP_011512374.1:p.Thr508=
XM_011514073.1:c.1524A>C	XP_011512375.1:p.Thr508=
XR_925638.1:n.1657A>C
NM_001330758.1:c.1524A>C	NP_001317687.1:p.Thr508=
XM_011514072.2:c.1524A>C	XP_011512374.1:p.Thr508=
XM_011514073.2:c.1524A>C	XP_011512375.1:p.Thr508=
XM_017009685.2:c.1524A>C	XP_016865174.1:p.Thr508=
XM_024446143.1:c.1380A>C	XP_024301911.1:p.Thr460=
XR_002956167.1:n.1571A>C
NM_004168.4:c.1524A>C MANE Select	NP_004159.2:p.Thr508=
NM_001294332.2:c.1380A>C	NP_001281261.1:p.Thr460=
NM_001330758.2:c.1524A>C	NP_001317687.1:p.Thr508=