Canonical Allele Identifier: CA373669762
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72820949C>A , CM000671.2:g.72820949C>A GRCh38
NC_000009.11:g.75435865C>A , CM000671.1:g.75435865C>A GRCh37
NC_000009.10:g.74625685C>A NCBI36
NG_008213.1:g.304149C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1871C>A MANE Select ENSP00000297784.6:p.Ala624Asp
ENST00000644967.1:c.*311C>A ENSP00000496159.1:n.*311C>A
ENST00000645053.1:c.1258-5920C>A ENSP00000493838.1:n.1258-5920C>A
ENST00000645208.2:c.1871C>A ENSP00000494684.1:p.Ala624Asp
ENST00000645773.1:c.1745C>A ENSP00000493698.1:p.Ala582Asp
ENST00000645787.1:n.2014C>A
ENST00000646619.1:c.1433C>A ENSP00000493726.1:p.Ala478Asp
ENST00000651183.1:c.1433C>A ENSP00000498723.1:p.Ala478Asp
ENST00000297784.9:c.1871C>A ENSP00000297784.5:p.Ala624Asp
ENST00000340019.4:c.1871C>A ENSP00000341433.3:p.Ala624Asp
ENST00000469455.1:n.352C>A
ENST00000486417.5:n.769C>A
NM_138691.2:c.1871C>A NP_619636.2:p.Ala624Asp
XM_011518213.1:c.2459C>A XP_011516515.1:p.Ala820Asp
XM_017014256.1:c.1874C>A XP_016869745.1:p.Ala625Asp
NM_138691.3:c.1871C>A MANE Select NP_619636.2:p.Ala624Asp