Canonical Allele Identifier: CA1855065589
Gene: TMC1 HGNC NCBI

Linked Data

dbSNP Id: rs1826522623

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72694859_72694862del , CM000671.2:g.72694859_72694862del GRCh38
NC_000009.11:g.75309775_75309778del , CM000671.1:g.75309775_75309778del GRCh37
NC_000009.10:g.74499595_74499598del NCBI36
NG_008213.1:g.178059_178062del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.236+145_236+148del MANE Select ENSP00000297784.6:n.236+145_236+148del
ENST00000644967.1:c.-77+145_-77+148del ENSP00000496159.1:n.-77+145_-77+148del
ENST00000645053.1:c.-77+145_-77+148del ENSP00000493838.1:n.-77+145_-77+148del
ENST00000645208.2:c.236+145_236+148del ENSP00000494684.1:n.236+145_236+148del
ENST00000645773.1:c.236+145_236+148del ENSP00000493698.1:n.236+145_236+148del
ENST00000645787.1:n.276+145_276+148del
ENST00000646244.1:n.686+145_686+148del
ENST00000646619.1:c.-77+145_-77+148del ENSP00000493726.1:n.-77+145_-77+148del
ENST00000650689.1:n.660+145_660+148del
ENST00000651183.1:c.-77+145_-77+148del ENSP00000498723.1:n.-77+145_-77+148del
ENST00000297784.9:c.236+145_236+148del ENSP00000297784.5:n.236+145_236+148del
ENST00000340019.4:c.236+145_236+148del ENSP00000341433.3:n.236+145_236+148del
NM_138691.2:c.236+145_236+148del NP_619636.2:n.236+145_236+148del
XM_011518213.1:c.824+145_824+148del XP_011516515.1:n.824+145_824+148del
XM_017014256.1:c.239+145_239+148del XP_016869745.1:n.239+145_239+148del
NM_138691.3:c.236+145_236+148del MANE Select NP_619636.2:n.236+145_236+148del