Canonical Allele Identifier: CA2615987292

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095213-TTATAAGACTCACAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095219_112095232del , CM000673.2:g.112095219_112095232del	GRCh38
NC_000011.9:g.111965943_111965956del , CM000673.1:g.111965943_111965956del	GRCh37
NC_000011.8:g.111471153_111471166del	NCBI36
NG_012337.2:g.13373_13386del
NG_012337.3:g.13373_13386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6208_314+6221del	ENSP00000433202.2:n.314+6208_314+6221del
ENST00000375549.8:c.*249_*262del MANE Select	ENSP00000364699.3:n.*249_*262del
ENST00000528021.6:c.314+6208_314+6221del	ENSP00000432465.1:n.314+6208_314+6221del
ENST00000375549.7:c.*249_*262del	ENSP00000364699.3:n.*249_*262del
ENST00000525291.5:c.*249_*262del	ENSP00000436669.1:n.*249_*262del
ENST00000525987.5:n.319+6208_319+6221del
ENST00000528021.5:c.314+6208_314+6221del	ENSP00000432465.1:n.314+6208_314+6221del
ENST00000528048.5:c.*326_*339del	ENSP00000436217.1:n.*326_*339del
ENST00000531744.5:c.314+6208_314+6221del	ENSP00000456957.1:n.314+6208_314+6221del
ENST00000532699.1:c.314+6208_314+6221del	ENSP00000456434.1:n.314+6208_314+6221del
ENST00000534010.1:c.145+6208_145+6221del
NM_001276503.1:c.*326_*339del	NP_001263432.1:n.*326_*339del
NM_001276504.1:c.*249_*262del	NP_001263433.1:n.*249_*262del
NM_001276506.1:c.*427_*440del	NP_001263435.1:n.*427_*440del
NM_003002.3:c.*249_*262del	NP_002993.1:n.*249_*262del
NR_077060.1:n.867_880del
NM_003002.4:c.*249_*262del MANE Select	NP_002993.1:n.*249_*262del
NM_001276503.2:c.*326_*339del	NP_001263432.1:n.*326_*339del
NM_001276504.2:c.*249_*262del	NP_001263433.1:n.*249_*262del
NM_001276506.2:c.*427_*440del	NP_001263435.1:n.*427_*440del
NR_077060.2:n.818_831del