Canonical Allele Identifier: CA2615986735

Gene: SDHD

Linked Data

• gnomAD v4: 11-112094776-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094777dup , CM000673.2:g.112094777dup	GRCh38
NC_000011.9:g.111965501dup , CM000673.1:g.111965501dup	GRCh37
NC_000011.8:g.111470711dup	NCBI36
NG_012337.2:g.12931dup
NG_012337.3:g.12931dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*54-28dup	ENSP00000432946.2:n.*54-28dup
ENST00000534010.2:c.314+5766dup	ENSP00000433202.2:n.314+5766dup
ENST00000375549.8:c.315-28dup MANE Select	ENSP00000364699.3:n.315-28dup
ENST00000528021.6:c.314+5766dup	ENSP00000432465.1:n.314+5766dup
ENST00000375549.7:c.315-28dup	ENSP00000364699.3:n.315-28dup
ENST00000525291.5:c.198-28dup	ENSP00000436669.1:n.198-28dup
ENST00000525987.5:n.319+5766dup
ENST00000526592.5:c.*13-28dup	ENSP00000432005.1:n.*13-28dup
ENST00000528021.5:c.314+5766dup	ENSP00000432465.1:n.314+5766dup
ENST00000528048.5:c.170-28dup	ENSP00000436217.1:n.170-28dup
ENST00000528182.5:c.308-28dup	ENSP00000435475.1:n.308-28dup
ENST00000530923.5:c.359-28dup
ENST00000531744.5:c.314+5766dup	ENSP00000456957.1:n.314+5766dup
ENST00000532699.1:c.314+5766dup	ENSP00000456434.1:n.314+5766dup
ENST00000534010.1:c.145+5766dup
NM_001276503.1:c.170-28dup	NP_001263432.1:n.170-28dup
NM_001276504.1:c.198-28dup	NP_001263433.1:n.198-28dup
NM_001276506.1:c.*13-28dup	NP_001263435.1:n.*13-28dup
NM_003002.3:c.315-28dup	NP_002993.1:n.315-28dup
NR_077060.1:n.453-28dup
NM_003002.4:c.315-28dup MANE Select	NP_002993.1:n.315-28dup
NM_001276503.2:c.170-28dup	NP_001263432.1:n.170-28dup
NM_001276504.2:c.198-28dup	NP_001263433.1:n.198-28dup
NM_001276506.2:c.*13-28dup	NP_001263435.1:n.*13-28dup
NR_077060.2:n.404-28dup