Canonical Allele Identifier: CA2695215340

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094898del , CM000673.2:g.112094898del	GRCh38
NC_000011.9:g.111965622del , CM000673.1:g.111965622del	GRCh37
NC_000011.8:g.111470832del	NCBI36
NG_012337.2:g.13052del
NG_012337.3:g.13052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*147del	ENSP00000432946.2:n.*147del
ENST00000534010.2:c.314+5887del	ENSP00000433202.2:n.314+5887del
ENST00000375549.8:c.408del MANE Select	ENSP00000364699.3:p.Phe136LeufsTer?
ENST00000528021.6:c.314+5887del	ENSP00000432465.1:n.314+5887del
ENST00000375549.7:c.408del	ENSP00000364699.3:p.Phe136LeufsTer?
ENST00000525291.5:c.291del	ENSP00000436669.1:p.Phe97LeufsTer?
ENST00000525987.5:n.319+5887del
ENST00000526592.5:c.*106del	ENSP00000432005.1:n.*106del
ENST00000528021.5:c.314+5887del	ENSP00000432465.1:n.314+5887del
ENST00000528048.5:c.*5del	ENSP00000436217.1:n.*5del
ENST00000528182.5:c.*5del	ENSP00000435475.1:n.*5del
ENST00000530923.5:c.452del
ENST00000531744.5:c.314+5887del	ENSP00000456957.1:n.314+5887del
ENST00000532699.1:c.314+5887del	ENSP00000456434.1:n.314+5887del
ENST00000534010.1:c.145+5887del
NM_001276503.1:c.*5del	NP_001263432.1:n.*5del
NM_001276504.1:c.291del	NP_001263433.1:p.Phe97LeufsTer?
NM_001276506.1:c.*106del	NP_001263435.1:n.*106del
NM_003002.3:c.408del	NP_002993.1:p.Phe136LeufsTer?
NR_077060.1:n.546del
NM_003002.4:c.408del MANE Select	NP_002993.1:p.Phe136LeufsTer?
NM_001276503.2:c.*5del	NP_001263432.1:n.*5del
NM_001276504.2:c.291del	NP_001263433.1:p.Phe97LeufsTer?
NM_001276506.2:c.*106del	NP_001263435.1:n.*106del
NR_077060.2:n.497del