Canonical Allele Identifier: CA382618715

Gene: SDHD

Linked Data

• ClinVar Variation Id: 2942563
• ClinVar RCV Id: RCV003807729
• gnomAD v4: 11-112094805-G-T
• MyVariant Identifiers: chr11:g.111965529G>T (hg19) ; chr11:g.112094805G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094805G>T , CM000673.2:g.112094805G>T	GRCh38
NC_000011.9:g.111965529G>T , CM000673.1:g.111965529G>T	GRCh37
NC_000011.8:g.111470739G>T	NCBI36
NG_012337.2:g.12959G>T
NG_012337.3:g.12959G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*54G>T	ENSP00000432946.2:n.*54G>T
ENST00000534010.2:c.314+5794G>T	ENSP00000433202.2:n.314+5794G>T
ENST00000375549.8:c.315G>T MANE Select	ENSP00000364699.3:p.Trp105Cys
ENST00000528021.6:c.314+5794G>T	ENSP00000432465.1:n.314+5794G>T
ENST00000375549.7:c.315G>T	ENSP00000364699.3:p.Trp105Cys
ENST00000525291.5:c.198G>T	ENSP00000436669.1:p.Trp66Cys
ENST00000525987.5:n.319+5794G>T
ENST00000526592.5:c.*13G>T	ENSP00000432005.1:n.*13G>T
ENST00000528021.5:c.314+5794G>T	ENSP00000432465.1:n.314+5794G>T
ENST00000528048.5:c.170G>T	ENSP00000436217.1:p.Trp57Leu
ENST00000528182.5:c.308G>T	ENSP00000435475.1:p.Gly103Val
ENST00000530923.5:c.359G>T
ENST00000531744.5:c.314+5794G>T	ENSP00000456957.1:n.314+5794G>T
ENST00000532699.1:c.314+5794G>T	ENSP00000456434.1:n.314+5794G>T
ENST00000534010.1:c.145+5794G>T
NM_001276503.1:c.170G>T	NP_001263432.1:p.Trp57Leu
NM_001276504.1:c.198G>T	NP_001263433.1:p.Trp66Cys
NM_001276506.1:c.*13G>T	NP_001263435.1:n.*13G>T
NM_003002.3:c.315G>T	NP_002993.1:p.Trp105Cys
NR_077060.1:n.453G>T
NM_003002.4:c.315G>T MANE Select	NP_002993.1:p.Trp105Cys
NM_001276503.2:c.170G>T	NP_001263432.1:p.Trp57Leu
NM_001276504.2:c.198G>T	NP_001263433.1:p.Trp66Cys
NM_001276506.2:c.*13G>T	NP_001263435.1:n.*13G>T
NR_077060.2:n.404G>T