Canonical Allele Identifier: CA373669785
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72820960A>G , CM000671.2:g.72820960A>G GRCh38
NC_000009.11:g.75435876A>G , CM000671.1:g.75435876A>G GRCh37
NC_000009.10:g.74625696A>G NCBI36
NG_008213.1:g.304160A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.1882A>G MANE Select ENSP00000297784.6:p.Lys628Glu
ENST00000644967.1:c.*322A>G ENSP00000496159.1:n.*322A>G
ENST00000645053.1:c.1258-5909A>G ENSP00000493838.1:n.1258-5909A>G
ENST00000645208.2:c.1882A>G ENSP00000494684.1:p.Lys628Glu
ENST00000645773.1:c.1756A>G ENSP00000493698.1:p.Lys586Glu
ENST00000645787.1:n.2025A>G
ENST00000646619.1:c.1444A>G ENSP00000493726.1:p.Lys482Glu
ENST00000651183.1:c.1444A>G ENSP00000498723.1:p.Lys482Glu
ENST00000297784.9:c.1882A>G ENSP00000297784.5:p.Lys628Glu
ENST00000340019.4:c.1882A>G ENSP00000341433.3:p.Lys628Glu
ENST00000469455.1:n.363A>G
ENST00000486417.5:n.780A>G
NM_138691.2:c.1882A>G NP_619636.2:p.Lys628Glu
XM_011518213.1:c.2470A>G XP_011516515.1:p.Lys824Glu
XM_017014256.1:c.1885A>G XP_016869745.1:p.Lys629Glu
NM_138691.3:c.1882A>G MANE Select NP_619636.2:p.Lys628Glu