Canonical Allele Identifier: CA2615987243

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095174-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095174_112095175insA , CM000673.2:g.112095174_112095175insA	GRCh38
NC_000011.9:g.111965898_111965899insA , CM000673.1:g.111965898_111965899insA	GRCh37
NC_000011.8:g.111471108_111471109insA	NCBI36
NG_012337.2:g.13328_13329insA
NG_012337.3:g.13328_13329insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6163_314+6164insA	ENSP00000433202.2:n.314+6163_314+6164insA
ENST00000375549.8:c.*204_*205insA MANE Select	ENSP00000364699.3:n.*204_*205insA
ENST00000528021.6:c.314+6163_314+6164insA	ENSP00000432465.1:n.314+6163_314+6164insA
ENST00000375549.7:c.*204_*205insA	ENSP00000364699.3:n.*204_*205insA
ENST00000525291.5:c.*204_*205insA	ENSP00000436669.1:n.*204_*205insA
ENST00000525987.5:n.319+6163_319+6164insA
ENST00000526592.5:c.*382_*383insA	ENSP00000432005.1:n.*382_*383insA
ENST00000528021.5:c.314+6163_314+6164insA	ENSP00000432465.1:n.314+6163_314+6164insA
ENST00000528048.5:c.*281_*282insA	ENSP00000436217.1:n.*281_*282insA
ENST00000528182.5:c.*281_*282insA	ENSP00000435475.1:n.*281_*282insA
ENST00000531744.5:c.314+6163_314+6164insA	ENSP00000456957.1:n.314+6163_314+6164insA
ENST00000532699.1:c.314+6163_314+6164insA	ENSP00000456434.1:n.314+6163_314+6164insA
ENST00000534010.1:c.145+6163_145+6164insA
NM_001276503.1:c.*281_*282insA	NP_001263432.1:n.*281_*282insA
NM_001276504.1:c.*204_*205insA	NP_001263433.1:n.*204_*205insA
NM_001276506.1:c.*382_*383insA	NP_001263435.1:n.*382_*383insA
NM_003002.3:c.*204_*205insA	NP_002993.1:n.*204_*205insA
NR_077060.1:n.822_823insA
NM_003002.4:c.*204_*205insA MANE Select	NP_002993.1:n.*204_*205insA
NM_001276503.2:c.*281_*282insA	NP_001263432.1:n.*281_*282insA
NM_001276504.2:c.*204_*205insA	NP_001263433.1:n.*204_*205insA
NM_001276506.2:c.*382_*383insA	NP_001263435.1:n.*382_*383insA
NR_077060.2:n.773_774insA