Canonical Allele Identifier: CA1855120705
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72821017T= , CM000671.2:g.72821017T= GRCh38
NC_000009.11:g.75435933T= , CM000671.1:g.75435933T= GRCh37
NC_000009.10:g.74625753T= NCBI36
NG_008213.1:g.304217T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1939T= MANE Select ENSP00000297784.6:p.Ser647=
ENST00000644967.1:c.*379T= ENSP00000496159.1:n.*379T=
ENST00000645053.1:c.1258-5852T= ENSP00000493838.1:n.1258-5852T=
ENST00000645208.2:c.1939T= ENSP00000494684.1:p.Ser647=
ENST00000645773.1:c.1813T= ENSP00000493698.1:p.Ser605=
ENST00000645787.1:n.2082T=
ENST00000646619.1:c.1501T= ENSP00000493726.1:p.Ser501=
ENST00000651183.1:c.1501T= ENSP00000498723.1:p.Ser501=
ENST00000297784.9:c.1939T= ENSP00000297784.5:p.Ser647=
ENST00000340019.4:c.1939T= ENSP00000341433.3:p.Ser647=
ENST00000469455.1:n.420T=
ENST00000486417.5:n.837T=
NM_138691.2:c.1939T= NP_619636.2:p.Ser647=
XM_011518213.1:c.2527T= XP_011516515.1:p.Ser843=
XM_017014256.1:c.1942T= XP_016869745.1:p.Ser648=
NM_138691.3:c.1939T= MANE Select NP_619636.2:p.Ser647=