Canonical Allele Identifier: CA1855015489
Gene: TMC1 HGNC NCBI

Linked Data

dbSNP Id: rs1824411181

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72577887_72577889del , CM000671.2:g.72577887_72577889del GRCh38
NC_000009.11:g.75192803_75192805del , CM000671.1:g.75192803_75192805del GRCh37
NC_000009.10:g.74382623_74382625del NCBI36
NG_008213.1:g.61087_61089del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.-427-15_-427-13del MANE Select ENSP00000297784.6:n.-427-15_-427-13del
ENST00000643676.1:n.307-38481_307-38479del
ENST00000645208.2:c.-442_-440del ENSP00000494684.1:n.-442_-440del
ENST00000650689.1:n.66-15_66-13del
ENST00000651183.1:c.-528-15_-528-13del ENSP00000498723.1:n.-528-15_-528-13del
ENST00000651743.1:n.116-15_116-13del
ENST00000297784.9:c.-427-15_-427-13del ENSP00000297784.5:n.-427-15_-427-13del
ENST00000497073.1:n.100_102del
NM_138691.2:c.-427-15_-427-13del NP_619636.2:n.-427-15_-427-13del
NM_138691.3:c.-427-15_-427-13del MANE Select NP_619636.2:n.-427-15_-427-13del