Canonical Allele Identifier: CA2000561880
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088896_112088898delinsACT , CM000673.2:g.112088896_112088898delinsACT GRCh38
NC_000011.9:g.111959620_111959622delinsACT , CM000673.1:g.111959620_111959622delinsACT GRCh37
NC_000011.8:g.111464830_111464832delinsACT NCBI36
NG_012337.2:g.7050_7052delinsACT
NG_033145.1:g.2901_2903delinsAGT
NG_012337.3:g.7050_7052delinsACT

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.199_201delinsACT ENSP00000432946.2:p.Thr67=
ENST00000534010.2:c.199_201delinsACT ENSP00000433202.2:p.Thr67=
ENST00000375549.8:c.199_201delinsACT MANE Select ENSP00000364699.3:p.Thr67=
ENST00000528021.6:c.199_201delinsACT ENSP00000432465.1:p.Thr67=
ENST00000640554.1:c.*271_*273delinsACT ENSP00000491141.1:n.*271_*273delinsACT
ENST00000375549.7:c.199_201delinsACT ENSP00000364699.3:p.Thr67=
ENST00000525291.5:c.82_84delinsACT ENSP00000436669.1:p.Thr28=
ENST00000525987.5:n.204_206delinsACT
ENST00000526592.5:c.199_201delinsACT ENSP00000432005.1:p.Thr67=
ENST00000528021.5:c.199_201delinsACT ENSP00000432465.1:p.Thr67=
ENST00000528048.5:c.169+923_169+925delinsACT ENSP00000436217.1:n.169+923_169+925delins...
ENST00000528182.5:c.199_201delinsACT ENSP00000435475.1:p.Thr67=
ENST00000530923.5:c.189_191delinsACT
ENST00000531744.5:c.199_201delinsACT ENSP00000456957.1:p.Thr67=
ENST00000532699.1:c.199_201delinsACT ENSP00000456434.1:p.Thr67=
ENST00000534010.1:c.30_32delinsACT
ENST00000614349.4:c.199_201delinsACT ENSP00000480666.1:p.Thr67=
NM_001276503.1:c.169+923_169+925delinsACT NP_001263432.1:n.169+923_169+925delinsACT...
NM_001276504.1:c.82_84delinsACT NP_001263433.1:p.Thr28=
NM_001276506.1:c.199_201delinsACT NP_001263435.1:p.Thr67=
NM_003002.3:c.199_201delinsACT NP_002993.1:p.Thr67=
NR_077060.1:n.283_285delinsACT
NM_003002.4:c.199_201delinsACT MANE Select NP_002993.1:p.Thr67=
NM_001276503.2:c.169+923_169+925delinsACT NP_001263432.1:n.169+923_169+925delinsACT...
NM_001276504.2:c.82_84delinsACT NP_001263433.1:p.Thr28=
NM_001276506.2:c.199_201delinsACT NP_001263435.1:p.Thr67=
NR_077060.2:n.234_236delinsACT