Canonical Allele Identifier: CA2000554381

Gene: SDHD

Linked Data

• dbSNP Id: rs1865820710

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095251del , CM000673.2:g.112095251del	GRCh38
NC_000011.9:g.111965975del , CM000673.1:g.111965975del	GRCh37
NC_000011.8:g.111471185del	NCBI36
NG_012337.2:g.13405del
NG_012337.3:g.13405del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6240del	ENSP00000433202.2:n.314+6240del
ENST00000375549.8:c.*281del MANE Select	ENSP00000364699.3:n.*281del
ENST00000528021.6:c.314+6240del	ENSP00000432465.1:n.314+6240del
ENST00000375549.7:c.*281del	ENSP00000364699.3:n.*281del
ENST00000525291.5:c.*281del	ENSP00000436669.1:n.*281del
ENST00000525987.5:n.319+6240del
ENST00000528021.5:c.314+6240del	ENSP00000432465.1:n.314+6240del
ENST00000528048.5:c.*358del	ENSP00000436217.1:n.*358del
ENST00000531744.5:c.314+6240del	ENSP00000456957.1:n.314+6240del
ENST00000532699.1:c.314+6240del	ENSP00000456434.1:n.314+6240del
ENST00000534010.1:c.145+6240del
NM_001276503.1:c.*358del	NP_001263432.1:n.*358del
NM_001276504.1:c.*281del	NP_001263433.1:n.*281del
NM_001276506.1:c.*459del	NP_001263435.1:n.*459del
NM_003002.3:c.*281del	NP_002993.1:n.*281del
NR_077060.1:n.899del
NM_003002.4:c.*281del MANE Select	NP_002993.1:n.*281del
NM_001276503.2:c.*358del	NP_001263432.1:n.*358del
NM_001276504.2:c.*281del	NP_001263433.1:n.*281del
NM_001276506.2:c.*459del	NP_001263435.1:n.*459del
NR_077060.2:n.850del