Canonical Allele Identifier: CA1855120711
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72821028T= , CM000671.2:g.72821028T= GRCh38
NC_000009.11:g.75435944T= , CM000671.1:g.75435944T= GRCh37
NC_000009.10:g.74625764T= NCBI36
NG_008213.1:g.304228T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1950T= MANE Select ENSP00000297784.6:p.Pro650=
ENST00000644967.1:c.*390T= ENSP00000496159.1:n.*390T=
ENST00000645053.1:c.1258-5841T= ENSP00000493838.1:n.1258-5841T=
ENST00000645208.2:c.1950T= ENSP00000494684.1:p.Pro650=
ENST00000645773.1:c.1824T= ENSP00000493698.1:p.Pro608=
ENST00000645787.1:n.2093T=
ENST00000646619.1:c.1512T= ENSP00000493726.1:p.Pro504=
ENST00000651183.1:c.1512T= ENSP00000498723.1:p.Pro504=
ENST00000297784.9:c.1950T= ENSP00000297784.5:p.Pro650=
ENST00000340019.4:c.1950T= ENSP00000341433.3:p.Pro650=
ENST00000469455.1:n.431T=
ENST00000486417.5:n.848T=
NM_138691.2:c.1950T= NP_619636.2:p.Pro650=
XM_011518213.1:c.2538T= XP_011516515.1:p.Pro846=
XM_017014256.1:c.1953T= XP_016869745.1:p.Pro651=
NM_138691.3:c.1950T= MANE Select NP_619636.2:p.Pro650=