Canonical Allele Identifier: CA2690286144
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72694489_72694494del , CM000671.2:g.72694489_72694494del GRCh38
NC_000009.11:g.75309405_75309410del , CM000671.1:g.75309405_75309410del GRCh37
NC_000009.10:g.74499225_74499230del NCBI36
NG_008213.1:g.177689_177694del

Transcript Alleles

HGVS Amino-acid change
ENST00000297784.10:c.65-54_65-49del MANE Select ENSP00000297784.6:n.65-54_65-49del
ENST00000644967.1:c.-248-54_-248-49del ENSP00000496159.1:n.-248-54_-248-49del
ENST00000645053.1:c.-248-54_-248-49del ENSP00000493838.1:n.-248-54_-248-49del
ENST00000645208.2:c.65-54_65-49del ENSP00000494684.1:n.65-54_65-49del
ENST00000645773.1:c.65-54_65-49del ENSP00000493698.1:n.65-54_65-49del
ENST00000645787.1:n.93-42_93-37del
ENST00000646244.1:n.515-54_515-49del
ENST00000646619.1:c.-248-54_-248-49del ENSP00000493726.1:n.-248-54_-248-49del
ENST00000650689.1:n.489-54_489-49del
ENST00000651183.1:c.-248-54_-248-49del ENSP00000498723.1:n.-248-54_-248-49del
ENST00000297784.9:c.65-54_65-49del ENSP00000297784.5:n.65-54_65-49del
ENST00000340019.4:c.65-54_65-49del ENSP00000341433.3:n.65-54_65-49del
NM_138691.2:c.65-54_65-49del NP_619636.2:n.65-54_65-49del
XM_011518213.1:c.653-54_653-49del XP_011516515.1:n.653-54_653-49del
XM_017014256.1:c.68-54_68-49del XP_016869745.1:n.68-54_68-49del
NM_138691.3:c.65-54_65-49del MANE Select NP_619636.2:n.65-54_65-49del