Canonical Allele Identifier: CA373669754
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72820946A>G , CM000671.2:g.72820946A>G GRCh38
NC_000009.11:g.75435862A>G , CM000671.1:g.75435862A>G GRCh37
NC_000009.10:g.74625682A>G NCBI36
NG_008213.1:g.304146A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1868A>G MANE Select ENSP00000297784.6:p.Glu623Gly
ENST00000644967.1:c.*308A>G ENSP00000496159.1:n.*308A>G
ENST00000645053.1:c.1258-5923A>G ENSP00000493838.1:n.1258-5923A>G
ENST00000645208.2:c.1868A>G ENSP00000494684.1:p.Glu623Gly
ENST00000645773.1:c.1742A>G ENSP00000493698.1:p.Glu581Gly
ENST00000645787.1:n.2011A>G
ENST00000646619.1:c.1430A>G ENSP00000493726.1:p.Glu477Gly
ENST00000651183.1:c.1430A>G ENSP00000498723.1:p.Glu477Gly
ENST00000297784.9:c.1868A>G ENSP00000297784.5:p.Glu623Gly
ENST00000340019.4:c.1868A>G ENSP00000341433.3:p.Glu623Gly
ENST00000469455.1:n.349A>G
ENST00000486417.5:n.766A>G
NM_138691.2:c.1868A>G NP_619636.2:p.Glu623Gly
XM_011518213.1:c.2456A>G XP_011516515.1:p.Glu819Gly
XM_017014256.1:c.1871A>G XP_016869745.1:p.Glu624Gly
NM_138691.3:c.1868A>G MANE Select NP_619636.2:p.Glu623Gly