Canonical Allele Identifier: CA1855015531
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72577991C= , CM000671.2:g.72577991C= GRCh38
NC_000009.11:g.75192907C= , CM000671.1:g.75192907C= GRCh37
NC_000009.10:g.74382727C= NCBI36
NG_008213.1:g.61191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.-338C= MANE Select ENSP00000297784.6:n.-338C=
ENST00000643676.1:n.307-38377C=
ENST00000645053.1:c.-582C= ENSP00000493838.1:n.-582C=
ENST00000645208.2:c.-338C= ENSP00000494684.1:n.-338C=
ENST00000645773.1:c.-338C= ENSP00000493698.1:n.-338C=
ENST00000646244.1:n.72C=
ENST00000650689.1:n.155C=
ENST00000651183.1:c.-439C= ENSP00000498723.1:n.-439C=
ENST00000651743.1:n.205C=
ENST00000297784.9:c.-338C= ENSP00000297784.5:n.-338C=
ENST00000497073.1:n.204C=
NM_138691.2:c.-338C= NP_619636.2:n.-338C=
NM_138691.3:c.-338C= MANE Select NP_619636.2:n.-338C=