Canonical Allele Identifier: CA373724387
Gene: TMC1 HGNC NCBI

Linked Data

dbSNP Id: rs1796993

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72700522G>C , CM000671.2:g.72700522G>C GRCh38
NC_000009.11:g.75315438G>C , CM000671.1:g.75315438G>C GRCh37
NC_000009.10:g.74505258G>C NCBI36
NG_008213.1:g.183722G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.241G>C MANE Select ENSP00000297784.6:p.Glu81Gln
ENST00000644967.1:c.-77+5808G>C ENSP00000496159.1:n.-77+5808G>C
ENST00000645053.1:c.-77+5808G>C ENSP00000493838.1:n.-77+5808G>C
ENST00000645208.2:c.241G>C ENSP00000494684.1:p.Glu81Gln
ENST00000645773.1:c.236+5808G>C ENSP00000493698.1:n.236+5808G>C
ENST00000645787.1:n.281G>C
ENST00000646244.1:n.691G>C
ENST00000646619.1:c.-77+5808G>C ENSP00000493726.1:n.-77+5808G>C
ENST00000650689.1:n.660+5808G>C
ENST00000651183.1:c.-77+5808G>C ENSP00000498723.1:n.-77+5808G>C
ENST00000297784.9:c.241G>C ENSP00000297784.5:p.Glu81Gln
ENST00000340019.4:c.241G>C ENSP00000341433.3:p.Glu81Gln
NM_138691.2:c.241G>C NP_619636.2:p.Glu81Gln
XM_011518213.1:c.829G>C XP_011516515.1:p.Glu277Gln
XM_017014256.1:c.244G>C XP_016869745.1:p.Glu82Gln
NM_138691.3:c.241G>C MANE Select NP_619636.2:p.Glu81Gln