Canonical Allele Identifier: CA2000554415

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095280_112095282delinsAAG , CM000673.2:g.112095280_112095282delinsAAG	GRCh38
NC_000011.9:g.111966004_111966006delinsAAG , CM000673.1:g.111966004_111966006delinsAAG	GRCh37
NC_000011.8:g.111471214_111471216delinsAAG	NCBI36
NG_012337.2:g.13434_13436delinsAAG
NG_012337.3:g.13434_13436delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6269_314+6271delinsAAG	ENSP00000433202.2:n.314+6269_314+6271delinsAAG
ENST00000375549.8:c.*310_*312delinsAAG MANE Select	ENSP00000364699.3:n.*310_*312delinsAAG
ENST00000528021.6:c.314+6269_314+6271delinsAAG	ENSP00000432465.1:n.314+6269_314+6271delinsAAG
ENST00000375549.7:c.*310_*312delinsAAG	ENSP00000364699.3:n.*310_*312delinsAAG
ENST00000525291.5:c.*310_*312delinsAAG	ENSP00000436669.1:n.*310_*312delinsAAG
ENST00000525987.5:n.319+6269_319+6271delinsAAG
ENST00000528021.5:c.314+6269_314+6271delinsAAG	ENSP00000432465.1:n.314+6269_314+6271delinsAAG
ENST00000528048.5:c.*387_*389delinsAAG	ENSP00000436217.1:n.*387_*389delinsAAG
ENST00000531744.5:c.314+6269_314+6271delinsAAG	ENSP00000456957.1:n.314+6269_314+6271delinsAAG
ENST00000532699.1:c.314+6269_314+6271delinsAAG	ENSP00000456434.1:n.314+6269_314+6271delinsAAG
ENST00000534010.1:c.145+6269_145+6271delinsAAG
NM_001276503.1:c.*387_*389delinsAAG	NP_001263432.1:n.*387_*389delinsAAG
NM_001276504.1:c.*310_*312delinsAAG	NP_001263433.1:n.*310_*312delinsAAG
NM_001276506.1:c.*488_*490delinsAAG	NP_001263435.1:n.*488_*490delinsAAG
NM_003002.3:c.*310_*312delinsAAG	NP_002993.1:n.*310_*312delinsAAG
NR_077060.1:n.928_930delinsAAG
NM_003002.4:c.*310_*312delinsAAG MANE Select	NP_002993.1:n.*310_*312delinsAAG
NM_001276503.2:c.*387_*389delinsAAG	NP_001263432.1:n.*387_*389delinsAAG
NM_001276504.2:c.*310_*312delinsAAG	NP_001263433.1:n.*310_*312delinsAAG
NM_001276506.2:c.*488_*490delinsAAG	NP_001263435.1:n.*488_*490delinsAAG
NR_077060.2:n.879_881delinsAAG