Canonical Allele Identifier: CA2690290033
Gene: TMC1 HGNC NCBI

Linked Data

gnomAD v4: 9-72821184-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72821184C>T , CM000671.2:g.72821184C>T GRCh38
NC_000009.11:g.75436100C>T , CM000671.1:g.75436100C>T GRCh37
NC_000009.10:g.74625920C>T NCBI36
NG_008213.1:g.304384C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.2003+103C>T MANE Select ENSP00000297784.6:n.2003+103C>T
ENST00000644967.1:c.*443+103C>T ENSP00000496159.1:n.*443+103C>T
ENST00000645053.1:c.1258-5685C>T ENSP00000493838.1:n.1258-5685C>T
ENST00000645208.2:c.2003+103C>T ENSP00000494684.1:n.2003+103C>T
ENST00000645773.1:c.1877+103C>T ENSP00000493698.1:n.1877+103C>T
ENST00000645787.1:n.2146+103C>T
ENST00000646619.1:c.1565+103C>T ENSP00000493726.1:n.1565+103C>T
ENST00000651183.1:c.1565+103C>T ENSP00000498723.1:n.1565+103C>T
ENST00000297784.9:c.2003+103C>T ENSP00000297784.5:n.2003+103C>T
ENST00000340019.4:c.2003+103C>T ENSP00000341433.3:n.2003+103C>T
ENST00000469455.1:n.484+103C>T
ENST00000486417.5:n.901+103C>T
NM_138691.2:c.2003+103C>T NP_619636.2:n.2003+103C>T
XM_011518213.1:c.2591+103C>T XP_011516515.1:n.2591+103C>T
XM_017014256.1:c.2006+103C>T XP_016869745.1:n.2006+103C>T
NM_138691.3:c.2003+103C>T MANE Select NP_619636.2:n.2003+103C>T