Canonical Allele Identifier: CA1855120661
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72820902C= , CM000671.2:g.72820902C= GRCh38
NC_000009.11:g.75435818C= , CM000671.1:g.75435818C= GRCh37
NC_000009.10:g.74625638C= NCBI36
NG_008213.1:g.304102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1824C= MANE Select ENSP00000297784.6:p.Ser608=
ENST00000644967.1:c.*264C= ENSP00000496159.1:n.*264C=
ENST00000645053.1:c.1258-5967C= ENSP00000493838.1:n.1258-5967C=
ENST00000645208.2:c.1824C= ENSP00000494684.1:p.Ser608=
ENST00000645773.1:c.1698C= ENSP00000493698.1:p.Ser566=
ENST00000645787.1:n.1967C=
ENST00000646619.1:c.1386C= ENSP00000493726.1:p.Ser462=
ENST00000651183.1:c.1386C= ENSP00000498723.1:p.Ser462=
ENST00000297784.9:c.1824C= ENSP00000297784.5:p.Ser608=
ENST00000340019.4:c.1824C= ENSP00000341433.3:p.Ser608=
ENST00000469455.1:n.305C=
ENST00000486417.5:n.722C=
NM_138691.2:c.1824C= NP_619636.2:p.Ser608=
XM_011518213.1:c.2412C= XP_011516515.1:p.Ser804=
XM_017014256.1:c.1827C= XP_016869745.1:p.Ser609=
NM_138691.3:c.1824C= MANE Select NP_619636.2:p.Ser608=