Canonical Allele Identifier: CA2000561976

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088961_112088976delinsCTCTGCGATGGACTAT , CM000673.2:g.112088961_112088976delinsCTCTGCGATGGACTAT	GRCh38
NC_000011.9:g.111959685_111959700delinsCTCTGCGATGGACTAT , CM000673.1:g.111959685_111959700delinsCTCTGCGATGGACTAT	GRCh37
NC_000011.8:g.111464895_111464910delinsCTCTGCGATGGACTAT	NCBI36
NG_012337.2:g.7115_7130delinsCTCTGCGATGGACTAT
NG_033145.1:g.2823_2838delinsATAGTCCATCGCAGAG
NG_012337.3:g.7115_7130delinsCTCTGCGATGGACTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000432946.2:p.Cys88=
ENST00000534010.2:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000433202.2:p.Cys88=
ENST00000375549.8:c.264_279delinsCTCTGCGATGGACTAT MANE Select	ENSP00000364699.3:p.Cys88=
ENST00000528021.6:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000432465.1:p.Cys88=
ENST00000640554.1:c.*336_*351delinsCTCTGCGATGGACTAT	ENSP00000491141.1:n.*336_*351delinsCTCTGCGATGGACTAT
ENST00000375549.7:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000364699.3:p.Cys88=
ENST00000525291.5:c.147_162delinsCTCTGCGATGGACTAT	ENSP00000436669.1:p.Cys49=
ENST00000525987.5:n.269_284delinsCTCTGCGATGGACTAT
ENST00000526592.5:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000432005.1:p.Cys88=
ENST00000528021.5:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000432465.1:p.Cys88=
ENST00000528048.5:c.169+988_169+1003delinsCTCTGCGATGGACTAT	ENSP00000436217.1:n.169+988_169+1003delinsCTCTGCGATGGACTAT
ENST00000528182.5:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000435475.1:p.Cys88=
ENST00000530923.5:c.254_269delinsCTCTGCGATGGACTAT
ENST00000531744.5:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000456957.1:p.Cys88=
ENST00000532699.1:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000456434.1:p.Cys88=
ENST00000534010.1:c.95_110delinsCTCTGCGATGGACTAT
ENST00000614349.4:c.264_279delinsCTCTGCGATGGACTAT	ENSP00000480666.1:p.Cys88=
NM_001276503.1:c.169+988_169+1003delinsCTCTGCGATGGACTAT	NP_001263432.1:n.169+988_169+1003delinsCTCTGCGATGGACTAT
NM_001276504.1:c.147_162delinsCTCTGCGATGGACTAT	NP_001263433.1:p.Cys49=
NM_001276506.1:c.264_279delinsCTCTGCGATGGACTAT	NP_001263435.1:p.Cys88=
NM_003002.3:c.264_279delinsCTCTGCGATGGACTAT	NP_002993.1:p.Cys88=
NR_077060.1:n.348_363delinsCTCTGCGATGGACTAT
NM_003002.4:c.264_279delinsCTCTGCGATGGACTAT MANE Select	NP_002993.1:p.Cys88=
NM_001276503.2:c.169+988_169+1003delinsCTCTGCGATGGACTAT	NP_001263432.1:n.169+988_169+1003delinsCTCTGCGATGGACTAT
NM_001276504.2:c.147_162delinsCTCTGCGATGGACTAT	NP_001263433.1:p.Cys49=
NM_001276506.2:c.264_279delinsCTCTGCGATGGACTAT	NP_001263435.1:p.Cys88=
NR_077060.2:n.299_314delinsCTCTGCGATGGACTAT