Canonical Allele Identifier: CA2579353995
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72694738C>G , CM000671.2:g.72694738C>G GRCh38
NC_000009.11:g.75309654C>G , CM000671.1:g.75309654C>G GRCh37
NC_000009.10:g.74499474C>G NCBI36
NG_008213.1:g.177938C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.236+24C>G MANE Select ENSP00000297784.6:n.236+24C>G
ENST00000644967.1:c.-77+24C>G ENSP00000496159.1:n.-77+24C>G
ENST00000645053.1:c.-77+24C>G ENSP00000493838.1:n.-77+24C>G
ENST00000645208.2:c.236+24C>G ENSP00000494684.1:n.236+24C>G
ENST00000645773.1:c.236+24C>G ENSP00000493698.1:n.236+24C>G
ENST00000645787.1:n.276+24C>G
ENST00000646244.1:n.686+24C>G
ENST00000646619.1:c.-77+24C>G ENSP00000493726.1:n.-77+24C>G
ENST00000650689.1:n.660+24C>G
ENST00000651183.1:c.-77+24C>G ENSP00000498723.1:n.-77+24C>G
ENST00000297784.9:c.236+24C>G ENSP00000297784.5:n.236+24C>G
ENST00000340019.4:c.236+24C>G ENSP00000341433.3:n.236+24C>G
NM_138691.2:c.236+24C>G NP_619636.2:n.236+24C>G
XM_011518213.1:c.824+24C>G XP_011516515.1:n.824+24C>G
XM_017014256.1:c.239+24C>G XP_016869745.1:n.239+24C>G
NM_138691.3:c.236+24C>G MANE Select NP_619636.2:n.236+24C>G