Canonical Allele Identifier: CA2000559485
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086841_112086842delinsTC , CM000673.2:g.112086841_112086842delinsTC GRCh38
NC_000011.9:g.111957565_111957566delinsTC , CM000673.1:g.111957565_111957566delinsTC GRCh37
NC_000011.8:g.111462775_111462776delinsTC NCBI36
NG_012337.2:g.4995_4996delinsTC
NG_033145.1:g.4957_4958delinsGA
NG_012337.3:g.4995_4996delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000640554.1:c.-67_-66delinsTC ENSP00000491141.1:n.-67_-66delinsTC
ENST00000375549.7:c.-67_-66delinsTC ENSP00000364699.3:n.-67_-66delinsTC
ENST00000614349.4:c.-67_-66delinsTC ENSP00000480666.1:n.-67_-66delinsTC
NM_001276503.1:c.-67_-66delinsTC NP_001263432.1:n.-67_-66delinsTC
NM_001276504.1:c.-67_-66delinsTC NP_001263433.1:n.-67_-66delinsTC
NM_001276506.1:c.-67_-66delinsTC NP_001263435.1:n.-67_-66delinsTC
NM_003002.3:c.-67_-66delinsTC NP_002993.1:n.-67_-66delinsTC
NR_077060.1:n.18_19delinsTC