Canonical Allele Identifier: CA2615982693

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086777_112086778insA , CM000673.2:g.112086777_112086778insA GRCh38
NC_000011.9:g.111957501_111957502insA , CM000673.1:g.111957501_111957502insA GRCh37
NC_000011.8:g.111462711_111462712insA NCBI36
NG_012337.2:g.4931_4932insA
NG_033145.1:g.5021_5022insT
NG_012337.3:g.4931_4932insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375549.7:c.-131_-130insA (SDHD) ENSP00000364699.3:n.-131_-130insA
ENST00000504148.2:c.-55_-54insT (TIMM8B) ENSP00000422122.2:n.-55_-54insT
ENST00000509359.6:c.-55_-54insT (TIMM8B) ENSP00000421964.2:n.-55_-54insT
ENST00000541231.1:c.-10_-9insT (TIMM8B) ENSP00000438455.1:n.-10_-9insT
NM_012459.2:c.-10_-9insT (TIMM8B) NP_036591.2:n.-10_-9insT
NR_028383.1:n.21_22insT (TIMM8B)