Canonical Allele Identifier: CA2690290019
Gene: TMC1 HGNC NCBI

Linked Data

dbSNP Id: rs2118300021
gnomAD v4: 9-72821169-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72821169C>T , CM000671.2:g.72821169C>T GRCh38
NC_000009.11:g.75436085C>T , CM000671.1:g.75436085C>T GRCh37
NC_000009.10:g.74625905C>T NCBI36
NG_008213.1:g.304369C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.2003+88C>T MANE Select ENSP00000297784.6:n.2003+88C>T
ENST00000644967.1:c.*443+88C>T ENSP00000496159.1:n.*443+88C>T
ENST00000645053.1:c.1258-5700C>T ENSP00000493838.1:n.1258-5700C>T
ENST00000645208.2:c.2003+88C>T ENSP00000494684.1:n.2003+88C>T
ENST00000645773.1:c.1877+88C>T ENSP00000493698.1:n.1877+88C>T
ENST00000645787.1:n.2146+88C>T
ENST00000646619.1:c.1565+88C>T ENSP00000493726.1:n.1565+88C>T
ENST00000651183.1:c.1565+88C>T ENSP00000498723.1:n.1565+88C>T
ENST00000297784.9:c.2003+88C>T ENSP00000297784.5:n.2003+88C>T
ENST00000340019.4:c.2003+88C>T ENSP00000341433.3:n.2003+88C>T
ENST00000469455.1:n.484+88C>T
ENST00000486417.5:n.901+88C>T
NM_138691.2:c.2003+88C>T NP_619636.2:n.2003+88C>T
XM_011518213.1:c.2591+88C>T XP_011516515.1:n.2591+88C>T
XM_017014256.1:c.2006+88C>T XP_016869745.1:n.2006+88C>T
NM_138691.3:c.2003+88C>T MANE Select NP_619636.2:n.2003+88C>T