Canonical Allele Identifier: CA2000554393

Gene: SDHD

Linked Data

• dbSNP Id: rs1865820902
• gnomAD v4: 11-112095258-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095261dup , CM000673.2:g.112095261dup	GRCh38
NC_000011.9:g.111965985dup , CM000673.1:g.111965985dup	GRCh37
NC_000011.8:g.111471195dup	NCBI36
NG_012337.2:g.13415dup
NG_012337.3:g.13415dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6250dup	ENSP00000433202.2:n.314+6250dup
ENST00000375549.8:c.*291dup MANE Select	ENSP00000364699.3:n.*291dup
ENST00000528021.6:c.314+6250dup	ENSP00000432465.1:n.314+6250dup
ENST00000375549.7:c.*291dup	ENSP00000364699.3:n.*291dup
ENST00000525291.5:c.*291dup	ENSP00000436669.1:n.*291dup
ENST00000525987.5:n.319+6250dup
ENST00000528021.5:c.314+6250dup	ENSP00000432465.1:n.314+6250dup
ENST00000528048.5:c.*368dup	ENSP00000436217.1:n.*368dup
ENST00000531744.5:c.314+6250dup	ENSP00000456957.1:n.314+6250dup
ENST00000532699.1:c.314+6250dup	ENSP00000456434.1:n.314+6250dup
ENST00000534010.1:c.145+6250dup
NM_001276503.1:c.*368dup	NP_001263432.1:n.*368dup
NM_001276504.1:c.*291dup	NP_001263433.1:n.*291dup
NM_001276506.1:c.*469dup	NP_001263435.1:n.*469dup
NM_003002.3:c.*291dup	NP_002993.1:n.*291dup
NR_077060.1:n.909dup
NM_003002.4:c.*291dup MANE Select	NP_002993.1:n.*291dup
NM_001276503.2:c.*368dup	NP_001263432.1:n.*368dup
NM_001276504.2:c.*291dup	NP_001263433.1:n.*291dup
NM_001276506.2:c.*469dup	NP_001263435.1:n.*469dup
NR_077060.2:n.860dup