Canonical Allele Identifier: CA1855015534
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72577998G= , CM000671.2:g.72577998G= GRCh38
NC_000009.11:g.75192914G= , CM000671.1:g.75192914G= GRCh37
NC_000009.10:g.74382734G= NCBI36
NG_008213.1:g.61198G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.-331G= MANE Select ENSP00000297784.6:n.-331G=
ENST00000643676.1:n.307-38370G=
ENST00000645053.1:c.-575G= ENSP00000493838.1:n.-575G=
ENST00000645208.2:c.-331G= ENSP00000494684.1:n.-331G=
ENST00000645773.1:c.-331G= ENSP00000493698.1:n.-331G=
ENST00000646244.1:n.79G=
ENST00000650689.1:n.162G=
ENST00000651183.1:c.-432G= ENSP00000498723.1:n.-432G=
ENST00000651743.1:n.212G=
ENST00000297784.9:c.-331G= ENSP00000297784.5:n.-331G=
ENST00000497073.1:n.211G=
NM_138691.2:c.-331G= NP_619636.2:n.-331G=
NM_138691.3:c.-331G= MANE Select NP_619636.2:n.-331G=