Canonical Allele Identifier: CA2690286352
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72700539_72700541del , CM000671.2:g.72700539_72700541del GRCh38
NC_000009.11:g.75315455_75315457del , CM000671.1:g.75315455_75315457del GRCh37
NC_000009.10:g.74505275_74505277del NCBI36
NG_008213.1:g.183739_183741del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.258_260del MANE Select ENSP00000297784.6:p.Glu87del
ENST00000644967.1:c.-77+5825_-77+5827del ENSP00000496159.1:n.-77+5825_-77+5827del
ENST00000645053.1:c.-77+5825_-77+5827del ENSP00000493838.1:n.-77+5825_-77+5827del
ENST00000645208.2:c.258_260del ENSP00000494684.1:p.Glu87del
ENST00000645773.1:c.236+5825_236+5827del ENSP00000493698.1:n.236+5825_236+5827del
ENST00000645787.1:n.298_300del
ENST00000646244.1:n.708_710del
ENST00000646619.1:c.-77+5825_-77+5827del ENSP00000493726.1:n.-77+5825_-77+5827del
ENST00000650689.1:n.660+5825_660+5827del
ENST00000651183.1:c.-77+5825_-77+5827del ENSP00000498723.1:n.-77+5825_-77+5827del
ENST00000297784.9:c.258_260del ENSP00000297784.5:p.Glu87del
ENST00000340019.4:c.258_260del ENSP00000341433.3:p.Glu87del
NM_138691.2:c.258_260del NP_619636.2:p.Glu87del
XM_011518213.1:c.846_848del XP_011516515.1:p.Glu283del
XM_017014256.1:c.261_263del XP_016869745.1:p.Glu88del
NM_138691.3:c.258_260del MANE Select NP_619636.2:p.Glu87del