Canonical Allele Identifier: CA671749422

Gene: SDHD

Linked Data

• dbSNP Id: rs1455803447
• MyVariant Identifiers: chr11:g.111964396del (hg19) ; chr11:g.112093672del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112093672del , CM000673.2:g.112093672del	GRCh38
NC_000011.9:g.111964396del , CM000673.1:g.111964396del	GRCh37
NC_000011.8:g.111469606del	NCBI36
NG_012337.2:g.11826del
NG_012337.3:g.11826del

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*54-1133del	ENSP00000432946.2:n.*54-1133del
ENST00000534010.2:c.314+4661del	ENSP00000433202.2:n.314+4661del
ENST00000375549.8:c.315-1133del MANE Select	ENSP00000364699.3:n.315-1133del
ENST00000528021.6:c.314+4661del	ENSP00000432465.1:n.314+4661del
ENST00000375549.7:c.315-1133del	ENSP00000364699.3:n.315-1133del
ENST00000525291.5:c.198-1133del	ENSP00000436669.1:n.198-1133del
ENST00000525987.5:n.319+4661del
ENST00000526592.5:c.*12+463del	ENSP00000432005.1:n.*12+463del
ENST00000528021.5:c.314+4661del	ENSP00000432465.1:n.314+4661del
ENST00000528048.5:c.170-1133del	ENSP00000436217.1:n.170-1133del
ENST00000528182.5:c.308-1133del	ENSP00000435475.1:n.308-1133del
ENST00000530923.5:c.359-1133del
ENST00000531744.5:c.314+4661del	ENSP00000456957.1:n.314+4661del
ENST00000532699.1:c.314+4661del	ENSP00000456434.1:n.314+4661del
ENST00000534010.1:c.145+4661del
NM_001276503.1:c.170-1133del	NP_001263432.1:n.170-1133del
NM_001276504.1:c.198-1133del	NP_001263433.1:n.198-1133del
NM_001276506.1:c.*12+463del	NP_001263435.1:n.*12+463del
NM_003002.3:c.315-1133del	NP_002993.1:n.315-1133del
NR_077060.1:n.453-1133del
NM_003002.4:c.315-1133del MANE Select	NP_002993.1:n.315-1133del
NM_001276503.2:c.170-1133del	NP_001263432.1:n.170-1133del
NM_001276504.2:c.198-1133del	NP_001263433.1:n.198-1133del
NM_001276506.2:c.*12+463del	NP_001263435.1:n.*12+463del
NR_077060.2:n.404-1133del