Canonical Allele Identifier: CA382618993

Gene: SDHD

Linked Data

• ClinVar Variation Id: 1733584
• ClinVar RCV Id: RCV002452475
• MyVariant Identifiers: chr11:g.111965578A>T (hg19) ; chr11:g.112094854A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094854A>T , CM000673.2:g.112094854A>T	GRCh38
NC_000011.9:g.111965578A>T , CM000673.1:g.111965578A>T	GRCh37
NC_000011.8:g.111470788A>T	NCBI36
NG_012337.2:g.13008A>T
NG_012337.3:g.13008A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*103A>T	ENSP00000432946.2:n.*103A>T
ENST00000534010.2:c.314+5843A>T	ENSP00000433202.2:n.314+5843A>T
ENST00000375549.8:c.364A>T MANE Select	ENSP00000364699.3:p.Lys122Ter
ENST00000528021.6:c.314+5843A>T	ENSP00000432465.1:n.314+5843A>T
ENST00000375549.7:c.364A>T	ENSP00000364699.3:p.Lys122Ter
ENST00000525291.5:c.247A>T	ENSP00000436669.1:p.Lys83Ter
ENST00000525987.5:n.319+5843A>T
ENST00000526592.5:c.*62A>T	ENSP00000432005.1:n.*62A>T
ENST00000528021.5:c.314+5843A>T	ENSP00000432465.1:n.314+5843A>T
ENST00000528048.5:c.219A>T	ENSP00000436217.1:p.Arg73Ser
ENST00000528182.5:c.357A>T	ENSP00000435475.1:p.Arg119Ser
ENST00000530923.5:c.408A>T
ENST00000531744.5:c.314+5843A>T	ENSP00000456957.1:n.314+5843A>T
ENST00000532699.1:c.314+5843A>T	ENSP00000456434.1:n.314+5843A>T
ENST00000534010.1:c.145+5843A>T
NM_001276503.1:c.219A>T	NP_001263432.1:p.Arg73Ser
NM_001276504.1:c.247A>T	NP_001263433.1:p.Lys83Ter
NM_001276506.1:c.*62A>T	NP_001263435.1:n.*62A>T
NM_003002.3:c.364A>T	NP_002993.1:p.Lys122Ter
NR_077060.1:n.502A>T
NM_003002.4:c.364A>T MANE Select	NP_002993.1:p.Lys122Ter
NM_001276503.2:c.219A>T	NP_001263432.1:p.Arg73Ser
NM_001276504.2:c.247A>T	NP_001263433.1:p.Lys83Ter
NM_001276506.2:c.*62A>T	NP_001263435.1:n.*62A>T
NR_077060.2:n.453A>T