Canonical Allele Identifier: CA2615987189

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095130-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095134del , CM000673.2:g.112095134del	GRCh38
NC_000011.9:g.111965858del , CM000673.1:g.111965858del	GRCh37
NC_000011.8:g.111471068del	NCBI36
NG_012337.2:g.13288del
NG_012337.3:g.13288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*383del	ENSP00000432946.2:n.*383del
ENST00000534010.2:c.314+6123del	ENSP00000433202.2:n.314+6123del
ENST00000375549.8:c.*164del MANE Select	ENSP00000364699.3:n.*164del
ENST00000528021.6:c.314+6123del	ENSP00000432465.1:n.314+6123del
ENST00000375549.7:c.*164del	ENSP00000364699.3:n.*164del
ENST00000525291.5:c.*164del	ENSP00000436669.1:n.*164del
ENST00000525987.5:n.319+6123del
ENST00000526592.5:c.*342del	ENSP00000432005.1:n.*342del
ENST00000528021.5:c.314+6123del	ENSP00000432465.1:n.314+6123del
ENST00000528048.5:c.*241del	ENSP00000436217.1:n.*241del
ENST00000528182.5:c.*241del	ENSP00000435475.1:n.*241del
ENST00000530923.5:c.688del
ENST00000531744.5:c.314+6123del	ENSP00000456957.1:n.314+6123del
ENST00000532699.1:c.314+6123del	ENSP00000456434.1:n.314+6123del
ENST00000534010.1:c.145+6123del
NM_001276503.1:c.*241del	NP_001263432.1:n.*241del
NM_001276504.1:c.*164del	NP_001263433.1:n.*164del
NM_001276506.1:c.*342del	NP_001263435.1:n.*342del
NM_003002.3:c.*164del	NP_002993.1:n.*164del
NR_077060.1:n.782del
NM_003002.4:c.*164del MANE Select	NP_002993.1:n.*164del
NM_001276503.2:c.*241del	NP_001263432.1:n.*241del
NM_001276504.2:c.*164del	NP_001263433.1:n.*164del
NM_001276506.2:c.*342del	NP_001263435.1:n.*342del
NR_077060.2:n.733del