Canonical Allele Identifier: CA373724477
Gene: TMC1 HGNC NCBI

Linked Data

gnomAD v4: 9-72700558-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72700558A>C , CM000671.2:g.72700558A>C GRCh38
NC_000009.11:g.75315474A>C , CM000671.1:g.75315474A>C GRCh37
NC_000009.10:g.74505294A>C NCBI36
NG_008213.1:g.183758A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.277A>C MANE Select ENSP00000297784.6:p.Lys93Gln
ENST00000644967.1:c.-77+5844A>C ENSP00000496159.1:n.-77+5844A>C
ENST00000645053.1:c.-77+5844A>C ENSP00000493838.1:n.-77+5844A>C
ENST00000645208.2:c.277A>C ENSP00000494684.1:p.Lys93Gln
ENST00000645773.1:c.236+5844A>C ENSP00000493698.1:n.236+5844A>C
ENST00000645787.1:n.317A>C
ENST00000646244.1:n.727A>C
ENST00000646619.1:c.-77+5844A>C ENSP00000493726.1:n.-77+5844A>C
ENST00000650689.1:n.660+5844A>C
ENST00000651183.1:c.-77+5844A>C ENSP00000498723.1:n.-77+5844A>C
ENST00000297784.9:c.277A>C ENSP00000297784.5:p.Lys93Gln
ENST00000340019.4:c.277A>C ENSP00000341433.3:p.Lys93Gln
NM_138691.2:c.277A>C NP_619636.2:p.Lys93Gln
XM_011518213.1:c.865A>C XP_011516515.1:p.Lys289Gln
XM_017014256.1:c.280A>C XP_016869745.1:p.Lys94Gln
NM_138691.3:c.277A>C MANE Select NP_619636.2:p.Lys93Gln