Canonical Allele Identifier: CA1855090095
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72751859G= , CM000671.2:g.72751859G= GRCh38
NC_000009.11:g.75366775G= , CM000671.1:g.75366775G= GRCh37
NC_000009.10:g.74556595G= NCBI36
NG_008213.1:g.235059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.545G= MANE Select ENSP00000297784.6:p.Gly182=
ENST00000644967.1:c.107G= ENSP00000496159.1:p.Gly36=
ENST00000645053.1:c.107G= ENSP00000493838.1:p.Gly36=
ENST00000645208.2:c.545G= ENSP00000494684.1:p.Gly182=
ENST00000645773.1:c.419G= ENSP00000493698.1:p.Gly140=
ENST00000645787.1:n.585G=
ENST00000646619.1:c.107G= ENSP00000493726.1:p.Gly36=
ENST00000650689.1:n.843G=
ENST00000651183.1:c.107G= ENSP00000498723.1:p.Gly36=
ENST00000297784.9:c.545G= ENSP00000297784.5:p.Gly182=
ENST00000340019.4:c.545G= ENSP00000341433.3:p.Gly182=
NM_138691.2:c.545G= NP_619636.2:p.Gly182=
XM_011518213.1:c.1133G= XP_011516515.1:p.Gly378=
XM_017014256.1:c.548G= XP_016869745.1:p.Gly183=
NM_138691.3:c.545G= MANE Select NP_619636.2:p.Gly182=