Canonical Allele Identifier: CA671750728

Gene: SDHD

Linked Data

• dbSNP Id: rs1455162991
• gnomAD v3: 11-112095284-GA-G
• gnomAD v4: 11-112095284-GA-G
• MyVariant Identifiers: chr11:g.111966009del (hg19) ; chr11:g.112095285del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095286del , CM000673.2:g.112095286del	GRCh38
NC_000011.9:g.111966010del , CM000673.1:g.111966010del	GRCh37
NC_000011.8:g.111471220del	NCBI36
NG_012337.2:g.13440del
NG_012337.3:g.13440del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6275del	ENSP00000433202.2:n.314+6275del
ENST00000375549.8:c.*316del MANE Select	ENSP00000364699.3:n.*316del
ENST00000528021.6:c.314+6275del	ENSP00000432465.1:n.314+6275del
ENST00000375549.7:c.*316del	ENSP00000364699.3:n.*316del
ENST00000525291.5:c.*316del	ENSP00000436669.1:n.*316del
ENST00000525987.5:n.319+6275del
ENST00000528021.5:c.314+6275del	ENSP00000432465.1:n.314+6275del
ENST00000528048.5:c.*393del	ENSP00000436217.1:n.*393del
ENST00000531744.5:c.314+6275del	ENSP00000456957.1:n.314+6275del
ENST00000532699.1:c.314+6275del	ENSP00000456434.1:n.314+6275del
ENST00000534010.1:c.145+6275del
NM_001276503.1:c.*393del	NP_001263432.1:n.*393del
NM_001276504.1:c.*316del	NP_001263433.1:n.*316del
NM_001276506.1:c.*494del	NP_001263435.1:n.*494del
NM_003002.3:c.*316del	NP_002993.1:n.*316del
NR_077060.1:n.934del
NM_003002.4:c.*316del MANE Select	NP_002993.1:n.*316del
NM_001276503.2:c.*393del	NP_001263432.1:n.*393del
NM_001276504.2:c.*316del	NP_001263433.1:n.*316del
NM_001276506.2:c.*494del	NP_001263435.1:n.*494del
NR_077060.2:n.885del