Canonical Allele Identifier: CA2000560532
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112087693_112087694delinsCT , CM000673.2:g.112087693_112087694delinsCT GRCh38
NC_000011.9:g.111958417_111958418delinsCT , CM000673.1:g.111958417_111958418delinsCT GRCh37
NC_000011.8:g.111463627_111463628delinsCT NCBI36
NG_012337.2:g.5847_5848delinsCT
NG_033145.1:g.4105_4106delinsAG
NG_012337.3:g.5847_5848delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.53-164_53-163delinsCT ENSP00000432946.2:n.53-164_53-163delinsCT
ENST00000534010.2:c.53-164_53-163delinsCT ENSP00000433202.2:n.53-164_53-163delinsCT
ENST00000375549.8:c.53-164_53-163delinsCT MANE Select ENSP00000364699.3:n.53-164_53-163delinsCT
ENST00000528021.6:c.53-164_53-163delinsCT ENSP00000432465.1:n.53-164_53-163delinsCT
ENST00000640554.1:c.53-164_53-163delinsCT ENSP00000491141.1:n.53-164_53-163delinsCT
ENST00000375549.7:c.53-164_53-163delinsCT ENSP00000364699.3:n.53-164_53-163delinsCT
ENST00000525291.5:c.52+734_52+735delinsCT ENSP00000436669.1:n.52+734_52+735delinsCT
ENST00000525987.5:n.58-164_58-163delinsCT
ENST00000526592.5:c.53-164_53-163delinsCT ENSP00000432005.1:n.53-164_53-163delinsCT
ENST00000528021.5:c.53-164_53-163delinsCT ENSP00000432465.1:n.53-164_53-163delinsCT
ENST00000528048.5:c.53-164_53-163delinsCT ENSP00000436217.1:n.53-164_53-163delinsCT
ENST00000528182.5:c.53-164_53-163delinsCT ENSP00000435475.1:n.53-164_53-163delinsCT
ENST00000530923.5:c.43-164_43-163delinsCT
ENST00000531744.5:c.53-164_53-163delinsCT ENSP00000456957.1:n.53-164_53-163delinsCT
ENST00000532699.1:c.53-164_53-163delinsCT ENSP00000456434.1:n.53-164_53-163delinsCT
ENST00000614349.4:c.53-164_53-163delinsCT ENSP00000480666.1:n.53-164_53-163delinsCT
NM_001276503.1:c.53-164_53-163delinsCT NP_001263432.1:n.53-164_53-163delinsCT
NM_001276504.1:c.52+734_52+735delinsCT NP_001263433.1:n.52+734_52+735delinsCT
NM_001276506.1:c.53-164_53-163delinsCT NP_001263435.1:n.53-164_53-163delinsCT
NM_003002.3:c.53-164_53-163delinsCT NP_002993.1:n.53-164_53-163delinsCT
NR_077060.1:n.137-164_137-163delinsCT
NM_003002.4:c.53-164_53-163delinsCT MANE Select NP_002993.1:n.53-164_53-163delinsCT
NM_001276503.2:c.53-164_53-163delinsCT NP_001263432.1:n.53-164_53-163delinsCT
NM_001276504.2:c.52+734_52+735delinsCT NP_001263433.1:n.52+734_52+735delinsCT
NM_001276506.2:c.53-164_53-163delinsCT NP_001263435.1:n.53-164_53-163delinsCT
NR_077060.2:n.88-164_88-163delinsCT