Canonical Allele Identifier: CA1855015532
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72577993G= , CM000671.2:g.72577993G= GRCh38
NC_000009.11:g.75192909G= , CM000671.1:g.75192909G= GRCh37
NC_000009.10:g.74382729G= NCBI36
NG_008213.1:g.61193G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.-336G= MANE Select ENSP00000297784.6:n.-336G=
ENST00000643676.1:n.307-38375G=
ENST00000645053.1:c.-580G= ENSP00000493838.1:n.-580G=
ENST00000645208.2:c.-336G= ENSP00000494684.1:n.-336G=
ENST00000645773.1:c.-336G= ENSP00000493698.1:n.-336G=
ENST00000646244.1:n.74G=
ENST00000650689.1:n.157G=
ENST00000651183.1:c.-437G= ENSP00000498723.1:n.-437G=
ENST00000651743.1:n.207G=
ENST00000297784.9:c.-336G= ENSP00000297784.5:n.-336G=
ENST00000497073.1:n.206G=
NM_138691.2:c.-336G= NP_619636.2:n.-336G=
NM_138691.3:c.-336G= MANE Select NP_619636.2:n.-336G=