Canonical Allele Identifier: CA1855065499
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72694612C= , CM000671.2:g.72694612C= GRCh38
NC_000009.11:g.75309528C= , CM000671.1:g.75309528C= GRCh37
NC_000009.10:g.74499348C= NCBI36
NG_008213.1:g.177812C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.134C= MANE Select ENSP00000297784.6:p.Thr45=
ENST00000644967.1:c.-179C= ENSP00000496159.1:n.-179C=
ENST00000645053.1:c.-179C= ENSP00000493838.1:n.-179C=
ENST00000645208.2:c.134C= ENSP00000494684.1:p.Thr45=
ENST00000645773.1:c.134C= ENSP00000493698.1:p.Thr45=
ENST00000645787.1:n.174C=
ENST00000646244.1:n.584C=
ENST00000646619.1:c.-179C= ENSP00000493726.1:n.-179C=
ENST00000650689.1:n.558C=
ENST00000651183.1:c.-179C= ENSP00000498723.1:n.-179C=
ENST00000297784.9:c.134C= ENSP00000297784.5:p.Thr45=
ENST00000340019.4:c.134C= ENSP00000341433.3:p.Thr45=
NM_138691.2:c.134C= NP_619636.2:p.Thr45=
XM_011518213.1:c.722C= XP_011516515.1:p.Thr241=
XM_017014256.1:c.137C= XP_016869745.1:p.Thr46=
NM_138691.3:c.134C= MANE Select NP_619636.2:p.Thr45=