Canonical Allele Identifier: CA1855107551
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72791932T= , CM000671.2:g.72791932T= GRCh38
NC_000009.11:g.75406848T= , CM000671.1:g.75406848T= GRCh37
NC_000009.10:g.74596668T= NCBI36
NG_008213.1:g.275132T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1271T= MANE Select ENSP00000297784.6:p.Phe424=
ENST00000644967.1:c.833T= ENSP00000496159.1:p.Phe278=
ENST00000645053.1:c.833T= ENSP00000493838.1:p.Phe278=
ENST00000645208.2:c.1271T= ENSP00000494684.1:p.Phe424=
ENST00000645773.1:c.1145T= ENSP00000493698.1:p.Phe382=
ENST00000645787.1:n.1311T=
ENST00000646619.1:c.833T= ENSP00000493726.1:p.Phe278=
ENST00000650689.1:n.1569T=
ENST00000651183.1:c.833T= ENSP00000498723.1:p.Phe278=
ENST00000297784.9:c.1271T= ENSP00000297784.5:p.Phe424=
ENST00000340019.4:c.1271T= ENSP00000341433.3:p.Phe424=
NM_138691.2:c.1271T= NP_619636.2:p.Phe424=
XM_011518213.1:c.1859T= XP_011516515.1:p.Phe620=
XM_017014256.1:c.1274T= XP_016869745.1:p.Phe425=
NM_138691.3:c.1271T= MANE Select NP_619636.2:p.Phe424=