Canonical Allele Identifier: CA5081791
Community Standard Title: NM_138691.3(TMC1):c.795A>C (p.Thr265=)
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72772466A>C , CM000671.2:g.72772466A>C GRCh38
NC_000009.11:g.75387382A>C , CM000671.1:g.75387382A>C GRCh37
NC_000009.10:g.74577202A>C NCBI36
NG_008213.1:g.255666A>C

Transcript Alleles

HGVS Amino-acid Change
NM_138691.3:c.795A>C MANE Select NP_619636.2:p.Thr265=
ENST00000297784.10:c.795A>C MANE Select ENSP00000297784.6:p.Thr265=
NM_138691.2:c.795A>C NP_619636.2:p.Thr265=
ENST00000297784.9:c.795A>C ENSP00000297784.5:p.Thr265=
ENST00000340019.4:c.795A>C ENSP00000341433.3:p.Thr265=
ENST00000644967.1:c.357A>C ENSP00000496159.1:p.Thr119=
ENST00000645053.1:c.357A>C ENSP00000493838.1:p.Thr119=
ENST00000645208.2:c.795A>C ENSP00000494684.1:p.Thr265=
ENST00000645773.1:c.669A>C ENSP00000493698.1:p.Thr223=
ENST00000645787.1:n.835A>C
ENST00000646619.1:c.357A>C ENSP00000493726.1:p.Thr119=
ENST00000650689.1:n.1093A>C
ENST00000651183.1:c.357A>C ENSP00000498723.1:p.Thr119=
XM_011518213.1:c.1383A>C XP_011516515.1:p.Thr461=
XM_017014256.1:c.798A>C XP_016869745.1:p.Thr266=