Canonical Allele Identifier: CA2000553979

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094872_112094873delinsCT , CM000673.2:g.112094872_112094873delinsCT	GRCh38
NC_000011.9:g.111965596_111965597delinsCT , CM000673.1:g.111965596_111965597delinsCT	GRCh37
NC_000011.8:g.111470806_111470807delinsCT	NCBI36
NG_012337.2:g.13026_13027delinsCT
NG_012337.3:g.13026_13027delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*121_*122delinsCT	ENSP00000432946.2:n.*121_*122delinsCT
ENST00000534010.2:c.314+5861_314+5862delinsCT	ENSP00000433202.2:n.314+5861_314+5862delinsCT
ENST00000375549.8:c.382_383delinsCT MANE Select	ENSP00000364699.3:p.Leu128=
ENST00000528021.6:c.314+5861_314+5862delinsCT	ENSP00000432465.1:n.314+5861_314+5862delinsCT
ENST00000375549.7:c.382_383delinsCT	ENSP00000364699.3:p.Leu128=
ENST00000525291.5:c.265_266delinsCT	ENSP00000436669.1:p.Leu89=
ENST00000525987.5:n.319+5861_319+5862delinsCT
ENST00000526592.5:c.*80_*81delinsCT	ENSP00000432005.1:n.*80_*81delinsCT
ENST00000528021.5:c.314+5861_314+5862delinsCT	ENSP00000432465.1:n.314+5861_314+5862delinsCT
ENST00000528048.5:c.237_238delinsCT	ENSP00000436217.1:p.Gly79=
ENST00000528182.5:c.375_376delinsCT	ENSP00000435475.1:p.Gly125=
ENST00000530923.5:c.426_427delinsCT
ENST00000531744.5:c.314+5861_314+5862delinsCT	ENSP00000456957.1:n.314+5861_314+5862delinsCT
ENST00000532699.1:c.314+5861_314+5862delinsCT	ENSP00000456434.1:n.314+5861_314+5862delinsCT
ENST00000534010.1:c.145+5861_145+5862delinsCT
NM_001276503.1:c.237_238delinsCT	NP_001263432.1:p.Gly79=
NM_001276504.1:c.265_266delinsCT	NP_001263433.1:p.Leu89=
NM_001276506.1:c.*80_*81delinsCT	NP_001263435.1:n.*80_*81delinsCT
NM_003002.3:c.382_383delinsCT	NP_002993.1:p.Leu128=
NR_077060.1:n.520_521delinsCT
NM_003002.4:c.382_383delinsCT MANE Select	NP_002993.1:p.Leu128=
NM_001276503.2:c.237_238delinsCT	NP_001263432.1:p.Gly79=
NM_001276504.2:c.265_266delinsCT	NP_001263433.1:p.Leu89=
NM_001276506.2:c.*80_*81delinsCT	NP_001263435.1:n.*80_*81delinsCT
NR_077060.2:n.471_472delinsCT