Canonical Allele Identifier: CA601745862

Gene: SDHD

Linked Data

• dbSNP Id: rs1291869098
• gnomAD v2: 11-111964316-C-CTTACATTACAATGCAAAAAATTTTACAT
• gnomAD v3: 11-112093592-C-CTTACATTACAATGCAAAAAATTTTACAT
• gnomAD v4: 11-112093592-C-CTTACATTACAATGCAAAAAATTTTACAT
• MyVariant Identifiers: chr11:g.111964316_111964317insTTACATTACAATGCAAAAAATTTTACAT (hg19) ; chr11:g.112093592_112093593insTTACATTACAATGCAAAAAATTTTACAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112093593_112093594insTACATTACAATGCAAAAAATTTTACATT , CM000673.2:g.112093593_112093594insTACATTACAATGCAAAAAATTTTACATT	GRCh38
NC_000011.9:g.111964317_111964318insTACATTACAATGCAAAAAATTTTACATT , CM000673.1:g.111964317_111964318insTACATTACAATGCAAAAAATTTTACATT	GRCh37
NC_000011.8:g.111469527_111469528insTACATTACAATGCAAAAAATTTTACATT	NCBI36
NG_012337.2:g.11747_11748insTACATTACAATGCAAAAAATTTTACATT
NG_012337.3:g.11747_11748insTACATTACAATGCAAAAAATTTTACATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*54-1212_*54-1211insTACATTACAATGCAAAAAATTTTACATT	ENSP00000432946.2:n.*54-1212_*54-1211insTACATTACAATGCAAAAAATT...
ENST00000534010.2:c.314+4582_314+4583insTACATTACAATGCAAAAAATTTTACATT	ENSP00000433202.2:n.314+4582_314+4583insTACATTACAATGCAAAAAATT...
ENST00000375549.8:c.315-1212_315-1211insTACATTACAATGCAAAAAATTTTACATT MANE Select	ENSP00000364699.3:n.315-1212_315-1211insTACATTACAATGCAAAAAATT...
ENST00000528021.6:c.314+4582_314+4583insTACATTACAATGCAAAAAATTTTACATT	ENSP00000432465.1:n.314+4582_314+4583insTACATTACAATGCAAAAAATT...
ENST00000375549.7:c.315-1212_315-1211insTACATTACAATGCAAAAAATTTTACATT	ENSP00000364699.3:n.315-1212_315-1211insTACATTACAATGCAAAAAATT...
ENST00000525291.5:c.198-1212_198-1211insTACATTACAATGCAAAAAATTTTACATT	ENSP00000436669.1:n.198-1212_198-1211insTACATTACAATGCAAAAAATT...
ENST00000525987.5:n.319+4582_319+4583insTACATTACAATGCAAAAAATTTTACATT
ENST00000526592.5:c.*12+384_*12+385insTACATTACAATGCAAAAAATTTTACATT	ENSP00000432005.1:n.*12+384_*12+385insTACATTACAATGCAAAAAATTTT...
ENST00000528021.5:c.314+4582_314+4583insTACATTACAATGCAAAAAATTTTACATT	ENSP00000432465.1:n.314+4582_314+4583insTACATTACAATGCAAAAAATT...
ENST00000528048.5:c.170-1212_170-1211insTACATTACAATGCAAAAAATTTTACATT	ENSP00000436217.1:n.170-1212_170-1211insTACATTACAATGCAAAAAATT...
ENST00000528182.5:c.308-1212_308-1211insTACATTACAATGCAAAAAATTTTACATT	ENSP00000435475.1:n.308-1212_308-1211insTACATTACAATGCAAAAAATT...
ENST00000530923.5:c.359-1212_359-1211insTACATTACAATGCAAAAAATTTTACATT
ENST00000531744.5:c.314+4582_314+4583insTACATTACAATGCAAAAAATTTTACATT	ENSP00000456957.1:n.314+4582_314+4583insTACATTACAATGCAAAAAATT...
ENST00000532699.1:c.314+4582_314+4583insTACATTACAATGCAAAAAATTTTACATT	ENSP00000456434.1:n.314+4582_314+4583insTACATTACAATGCAAAAAATT...
ENST00000534010.1:c.145+4582_145+4583insTACATTACAATGCAAAAAATTTTACATT
NM_001276503.1:c.170-1212_170-1211insTACATTACAATGCAAAAAATTTTACATT	NP_001263432.1:n.170-1212_170-1211insTACATTACAATGCAAAAAATTTTA...
NM_001276504.1:c.198-1212_198-1211insTACATTACAATGCAAAAAATTTTACATT	NP_001263433.1:n.198-1212_198-1211insTACATTACAATGCAAAAAATTTTA...
NM_001276506.1:c.*12+384_*12+385insTACATTACAATGCAAAAAATTTTACATT	NP_001263435.1:n.*12+384_*12+385insTACATTACAATGCAAAAAATTTTACA...
NM_003002.3:c.315-1212_315-1211insTACATTACAATGCAAAAAATTTTACATT	NP_002993.1:n.315-1212_315-1211insTACATTACAATGCAAAAAATTTTACAT...
NR_077060.1:n.453-1212_453-1211insTACATTACAATGCAAAAAATTTTACATT
NM_003002.4:c.315-1212_315-1211insTACATTACAATGCAAAAAATTTTACATT MANE Select	NP_002993.1:n.315-1212_315-1211insTACATTACAATGCAAAAAATTTTACAT...
NM_001276503.2:c.170-1212_170-1211insTACATTACAATGCAAAAAATTTTACATT	NP_001263432.1:n.170-1212_170-1211insTACATTACAATGCAAAAAATTTTA...
NM_001276504.2:c.198-1212_198-1211insTACATTACAATGCAAAAAATTTTACATT	NP_001263433.1:n.198-1212_198-1211insTACATTACAATGCAAAAAATTTTA...
NM_001276506.2:c.*12+384_*12+385insTACATTACAATGCAAAAAATTTTACATT	NP_001263435.1:n.*12+384_*12+385insTACATTACAATGCAAAAAATTTTACA...
NR_077060.2:n.404-1212_404-1211insTACATTACAATGCAAAAAATTTTACATT