Canonical Allele Identifier: CA1855107547
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72791924A= , CM000671.2:g.72791924A= GRCh38
NC_000009.11:g.75406840A= , CM000671.1:g.75406840A= GRCh37
NC_000009.10:g.74596660A= NCBI36
NG_008213.1:g.275124A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1263A= MANE Select ENSP00000297784.6:p.Pro421=
ENST00000644967.1:c.825A= ENSP00000496159.1:p.Pro275=
ENST00000645053.1:c.825A= ENSP00000493838.1:p.Pro275=
ENST00000645208.2:c.1263A= ENSP00000494684.1:p.Pro421=
ENST00000645773.1:c.1137A= ENSP00000493698.1:p.Pro379=
ENST00000645787.1:n.1303A=
ENST00000646619.1:c.825A= ENSP00000493726.1:p.Pro275=
ENST00000650689.1:n.1561A=
ENST00000651183.1:c.825A= ENSP00000498723.1:p.Pro275=
ENST00000297784.9:c.1263A= ENSP00000297784.5:p.Pro421=
ENST00000340019.4:c.1263A= ENSP00000341433.3:p.Pro421=
NM_138691.2:c.1263A= NP_619636.2:p.Pro421=
XM_011518213.1:c.1851A= XP_011516515.1:p.Pro617=
XM_017014256.1:c.1266A= XP_016869745.1:p.Pro422=
NM_138691.3:c.1263A= MANE Select NP_619636.2:p.Pro421=