Canonical Allele Identifier: CA2000562035
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088973_112088976delinsCTAT , CM000673.2:g.112088973_112088976delinsCTAT GRCh38
NC_000011.9:g.111959697_111959700delinsCTAT , CM000673.1:g.111959697_111959700delinsCTAT GRCh37
NC_000011.8:g.111464907_111464910delinsCTAT NCBI36
NG_012337.2:g.7127_7130delinsCTAT
NG_033145.1:g.2823_2826delinsATAG
NG_012337.3:g.7127_7130delinsCTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.276_279delinsCTAT ENSP00000432946.2:p.Asp92=
ENST00000534010.2:c.276_279delinsCTAT ENSP00000433202.2:p.Asp92=
ENST00000375549.8:c.276_279delinsCTAT MANE Select ENSP00000364699.3:p.Asp92=
ENST00000528021.6:c.276_279delinsCTAT ENSP00000432465.1:p.Asp92=
ENST00000640554.1:c.*348_*351delinsCTAT ENSP00000491141.1:n.*348_*351delinsCTAT
ENST00000375549.7:c.276_279delinsCTAT ENSP00000364699.3:p.Asp92=
ENST00000525291.5:c.159_162delinsCTAT ENSP00000436669.1:p.Asp53=
ENST00000525987.5:n.281_284delinsCTAT
ENST00000526592.5:c.276_279delinsCTAT ENSP00000432005.1:p.Asp92=
ENST00000528021.5:c.276_279delinsCTAT ENSP00000432465.1:p.Asp92=
ENST00000528048.5:c.169+1000_169+1003delinsCTAT ENSP00000436217.1:n.169+1000_169+1003deli...
ENST00000528182.5:c.276_279delinsCTAT ENSP00000435475.1:p.Asp92=
ENST00000530923.5:c.266_269delinsCTAT
ENST00000531744.5:c.276_279delinsCTAT ENSP00000456957.1:p.Asp92=
ENST00000532699.1:c.276_279delinsCTAT ENSP00000456434.1:p.Asp92=
ENST00000534010.1:c.107_110delinsCTAT
ENST00000614349.4:c.276_279delinsCTAT ENSP00000480666.1:p.Asp92=
NM_001276503.1:c.169+1000_169+1003delinsCTAT NP_001263432.1:n.169+1000_169+1003delinsC...
NM_001276504.1:c.159_162delinsCTAT NP_001263433.1:p.Asp53=
NM_001276506.1:c.276_279delinsCTAT NP_001263435.1:p.Asp92=
NM_003002.3:c.276_279delinsCTAT NP_002993.1:p.Asp92=
NR_077060.1:n.360_363delinsCTAT
NM_003002.4:c.276_279delinsCTAT MANE Select NP_002993.1:p.Asp92=
NM_001276503.2:c.169+1000_169+1003delinsCTAT NP_001263432.1:n.169+1000_169+1003delinsC...
NM_001276504.2:c.159_162delinsCTAT NP_001263433.1:p.Asp53=
NM_001276506.2:c.276_279delinsCTAT NP_001263435.1:p.Asp92=
NR_077060.2:n.311_314delinsCTAT