Canonical Allele Identifier: CA2000561943
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088937_112088938delinsTC , CM000673.2:g.112088937_112088938delinsTC GRCh38
NC_000011.9:g.111959661_111959662delinsTC , CM000673.1:g.111959661_111959662delinsTC GRCh37
NC_000011.8:g.111464871_111464872delinsTC NCBI36
NG_012337.2:g.7091_7092delinsTC
NG_033145.1:g.2861_2862delinsGA
NG_012337.3:g.7091_7092delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.240_241delinsTC ENSP00000432946.2:p.Leu80=
ENST00000534010.2:c.240_241delinsTC ENSP00000433202.2:p.Leu80=
ENST00000375549.8:c.240_241delinsTC MANE Select ENSP00000364699.3:p.Leu80=
ENST00000528021.6:c.240_241delinsTC ENSP00000432465.1:p.Leu80=
ENST00000640554.1:c.*312_*313delinsTC ENSP00000491141.1:n.*312_*313delinsTC
ENST00000375549.7:c.240_241delinsTC ENSP00000364699.3:p.Leu80=
ENST00000525291.5:c.123_124delinsTC ENSP00000436669.1:p.Leu41=
ENST00000525987.5:n.245_246delinsTC
ENST00000526592.5:c.240_241delinsTC ENSP00000432005.1:p.Leu80=
ENST00000528021.5:c.240_241delinsTC ENSP00000432465.1:p.Leu80=
ENST00000528048.5:c.169+964_169+965delinsTC ENSP00000436217.1:n.169+964_169+965delinsTC
ENST00000528182.5:c.240_241delinsTC ENSP00000435475.1:p.Leu80=
ENST00000530923.5:c.230_231delinsTC
ENST00000531744.5:c.240_241delinsTC ENSP00000456957.1:p.Leu80=
ENST00000532699.1:c.240_241delinsTC ENSP00000456434.1:p.Leu80=
ENST00000534010.1:c.71_72delinsTC
ENST00000614349.4:c.240_241delinsTC ENSP00000480666.1:p.Leu80=
NM_001276503.1:c.169+964_169+965delinsTC NP_001263432.1:n.169+964_169+965delinsTC
NM_001276504.1:c.123_124delinsTC NP_001263433.1:p.Leu41=
NM_001276506.1:c.240_241delinsTC NP_001263435.1:p.Leu80=
NM_003002.3:c.240_241delinsTC NP_002993.1:p.Leu80=
NR_077060.1:n.324_325delinsTC
NM_003002.4:c.240_241delinsTC MANE Select NP_002993.1:p.Leu80=
NM_001276503.2:c.169+964_169+965delinsTC NP_001263432.1:n.169+964_169+965delinsTC
NM_001276504.2:c.123_124delinsTC NP_001263433.1:p.Leu41=
NM_001276506.2:c.240_241delinsTC NP_001263435.1:p.Leu80=
NR_077060.2:n.275_276delinsTC