Canonical Allele Identifier: CA2690288386
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72791832_72791834del , CM000671.2:g.72791832_72791834del GRCh38
NC_000009.11:g.75406748_75406750del , CM000671.1:g.75406748_75406750del GRCh37
NC_000009.10:g.74596568_74596570del NCBI36
NG_008213.1:g.275032_275034del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1225-54_1225-52del MANE Select ENSP00000297784.6:n.1225-54_1225-52del
ENST00000644967.1:c.787-54_787-52del ENSP00000496159.1:n.787-54_787-52del
ENST00000645053.1:c.787-54_787-52del ENSP00000493838.1:n.787-54_787-52del
ENST00000645208.2:c.1225-54_1225-52del ENSP00000494684.1:n.1225-54_1225-52del
ENST00000645773.1:c.1099-54_1099-52del ENSP00000493698.1:n.1099-54_1099-52del
ENST00000645787.1:n.1265-54_1265-52del
ENST00000646619.1:c.787-54_787-52del ENSP00000493726.1:n.787-54_787-52del
ENST00000650689.1:n.1523-54_1523-52del
ENST00000651183.1:c.787-54_787-52del ENSP00000498723.1:n.787-54_787-52del
ENST00000297784.9:c.1225-54_1225-52del ENSP00000297784.5:n.1225-54_1225-52del
ENST00000340019.4:c.1225-54_1225-52del ENSP00000341433.3:n.1225-54_1225-52del
NM_138691.2:c.1225-54_1225-52del NP_619636.2:n.1225-54_1225-52del
XM_011518213.1:c.1813-54_1813-52del XP_011516515.1:n.1813-54_1813-52del
XM_017014256.1:c.1228-54_1228-52del XP_016869745.1:n.1228-54_1228-52del
NM_138691.3:c.1225-54_1225-52del MANE Select NP_619636.2:n.1225-54_1225-52del