Canonical Allele Identifier: CA671750646

Gene: SDHD

Linked Data

• dbSNP Id: rs1183512273
• gnomAD v3: 11-112095203-TC-T
• gnomAD v4: 11-112095203-TC-T
• MyVariant Identifiers: chr11:g.111965928del (hg19) ; chr11:g.112095204del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095206del , CM000673.2:g.112095206del	GRCh38
NC_000011.9:g.111965930del , CM000673.1:g.111965930del	GRCh37
NC_000011.8:g.111471140del	NCBI36
NG_012337.2:g.13360del
NG_012337.3:g.13360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6195del	ENSP00000433202.2:n.314+6195del
ENST00000375549.8:c.*236del MANE Select	ENSP00000364699.3:n.*236del
ENST00000528021.6:c.314+6195del	ENSP00000432465.1:n.314+6195del
ENST00000375549.7:c.*236del	ENSP00000364699.3:n.*236del
ENST00000525291.5:c.*236del	ENSP00000436669.1:n.*236del
ENST00000525987.5:n.319+6195del
ENST00000526592.5:c.*414del	ENSP00000432005.1:n.*414del
ENST00000528021.5:c.314+6195del	ENSP00000432465.1:n.314+6195del
ENST00000528048.5:c.*313del	ENSP00000436217.1:n.*313del
ENST00000528182.5:c.*313del	ENSP00000435475.1:n.*313del
ENST00000531744.5:c.314+6195del	ENSP00000456957.1:n.314+6195del
ENST00000532699.1:c.314+6195del	ENSP00000456434.1:n.314+6195del
ENST00000534010.1:c.145+6195del
NM_001276503.1:c.*313del	NP_001263432.1:n.*313del
NM_001276504.1:c.*236del	NP_001263433.1:n.*236del
NM_001276506.1:c.*414del	NP_001263435.1:n.*414del
NM_003002.3:c.*236del	NP_002993.1:n.*236del
NR_077060.1:n.854del
NM_003002.4:c.*236del MANE Select	NP_002993.1:n.*236del
NM_001276503.2:c.*313del	NP_001263432.1:n.*313del
NM_001276504.2:c.*236del	NP_001263433.1:n.*236del
NM_001276506.2:c.*414del	NP_001263435.1:n.*414del
NR_077060.2:n.805del