Canonical Allele Identifier: CA2615987137

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095089-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095090_112095092del , CM000673.2:g.112095090_112095092del	GRCh38
NC_000011.9:g.111965814_111965816del , CM000673.1:g.111965814_111965816del	GRCh37
NC_000011.8:g.111471024_111471026del	NCBI36
NG_012337.2:g.13244_13246del
NG_012337.3:g.13244_13246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*339_*341del	ENSP00000432946.2:n.*339_*341del
ENST00000534010.2:c.314+6079_314+6081del	ENSP00000433202.2:n.314+6079_314+6081del
ENST00000375549.8:c.*120_*122del MANE Select	ENSP00000364699.3:n.*120_*122del
ENST00000528021.6:c.314+6079_314+6081del	ENSP00000432465.1:n.314+6079_314+6081del
ENST00000375549.7:c.*120_*122del	ENSP00000364699.3:n.*120_*122del
ENST00000525291.5:c.*120_*122del	ENSP00000436669.1:n.*120_*122del
ENST00000525987.5:n.319+6079_319+6081del
ENST00000526592.5:c.*298_*300del	ENSP00000432005.1:n.*298_*300del
ENST00000528021.5:c.314+6079_314+6081del	ENSP00000432465.1:n.314+6079_314+6081del
ENST00000528048.5:c.*197_*199del	ENSP00000436217.1:n.*197_*199del
ENST00000528182.5:c.*197_*199del	ENSP00000435475.1:n.*197_*199del
ENST00000530923.5:c.644_646del
ENST00000531744.5:c.314+6079_314+6081del	ENSP00000456957.1:n.314+6079_314+6081del
ENST00000532699.1:c.314+6079_314+6081del	ENSP00000456434.1:n.314+6079_314+6081del
ENST00000534010.1:c.145+6079_145+6081del
NM_001276503.1:c.*197_*199del	NP_001263432.1:n.*197_*199del
NM_001276504.1:c.*120_*122del	NP_001263433.1:n.*120_*122del
NM_001276506.1:c.*298_*300del	NP_001263435.1:n.*298_*300del
NM_003002.3:c.*120_*122del	NP_002993.1:n.*120_*122del
NR_077060.1:n.738_740del
NM_003002.4:c.*120_*122del MANE Select	NP_002993.1:n.*120_*122del
NM_001276503.2:c.*197_*199del	NP_001263432.1:n.*197_*199del
NM_001276504.2:c.*120_*122del	NP_001263433.1:n.*120_*122del
NM_001276506.2:c.*298_*300del	NP_001263435.1:n.*298_*300del
NR_077060.2:n.689_691del