Canonical Allele Identifier: CA373723714
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72694585A>C , CM000671.2:g.72694585A>C GRCh38
NC_000009.11:g.75309501A>C , CM000671.1:g.75309501A>C GRCh37
NC_000009.10:g.74499321A>C NCBI36
NG_008213.1:g.177785A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297784.10:c.107A>C MANE Select ENSP00000297784.6:p.Glu36Ala
ENST00000644967.1:c.-206A>C ENSP00000496159.1:n.-206A>C
ENST00000645053.1:c.-206A>C ENSP00000493838.1:n.-206A>C
ENST00000645208.2:c.107A>C ENSP00000494684.1:p.Glu36Ala
ENST00000645773.1:c.107A>C ENSP00000493698.1:p.Glu36Ala
ENST00000645787.1:n.147A>C
ENST00000646244.1:n.557A>C
ENST00000646619.1:c.-206A>C ENSP00000493726.1:n.-206A>C
ENST00000650689.1:n.531A>C
ENST00000651183.1:c.-206A>C ENSP00000498723.1:n.-206A>C
ENST00000297784.9:c.107A>C ENSP00000297784.5:p.Glu36Ala
ENST00000340019.4:c.107A>C ENSP00000341433.3:p.Glu36Ala
NM_138691.2:c.107A>C NP_619636.2:p.Glu36Ala
XM_011518213.1:c.695A>C XP_011516515.1:p.Glu232Ala
XM_017014256.1:c.110A>C XP_016869745.1:p.Glu37Ala
NM_138691.3:c.107A>C MANE Select NP_619636.2:p.Glu36Ala