Canonical Allele Identifier: CA2690284782
Gene: TMC1 HGNC NCBI

Linked Data

gnomAD v4: 9-72577990-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72577990C>A , CM000671.2:g.72577990C>A GRCh38
NC_000009.11:g.75192906C>A , CM000671.1:g.75192906C>A GRCh37
NC_000009.10:g.74382726C>A NCBI36
NG_008213.1:g.61190C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.-339C>A MANE Select ENSP00000297784.6:n.-339C>A
ENST00000643676.1:n.307-38378C>A
ENST00000645053.1:c.-583C>A ENSP00000493838.1:n.-583C>A
ENST00000645208.2:c.-339C>A ENSP00000494684.1:n.-339C>A
ENST00000645773.1:c.-339C>A ENSP00000493698.1:n.-339C>A
ENST00000646244.1:n.71C>A
ENST00000650689.1:n.154C>A
ENST00000651183.1:c.-440C>A ENSP00000498723.1:n.-440C>A
ENST00000651743.1:n.204C>A
ENST00000297784.9:c.-339C>A ENSP00000297784.5:n.-339C>A
ENST00000497073.1:n.203C>A
NM_138691.2:c.-339C>A NP_619636.2:n.-339C>A
NM_138691.3:c.-339C>A MANE Select NP_619636.2:n.-339C>A