Canonical Allele Identifier: CA373724490
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72700562C>A , CM000671.2:g.72700562C>A GRCh38
NC_000009.11:g.75315478C>A , CM000671.1:g.75315478C>A GRCh37
NC_000009.10:g.74505298C>A NCBI36
NG_008213.1:g.183762C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.281C>A MANE Select ENSP00000297784.6:p.Ala94Glu
ENST00000644967.1:c.-77+5848C>A ENSP00000496159.1:n.-77+5848C>A
ENST00000645053.1:c.-77+5848C>A ENSP00000493838.1:n.-77+5848C>A
ENST00000645208.2:c.281C>A ENSP00000494684.1:p.Ala94Glu
ENST00000645773.1:c.236+5848C>A ENSP00000493698.1:n.236+5848C>A
ENST00000645787.1:n.321C>A
ENST00000646244.1:n.731C>A
ENST00000646619.1:c.-77+5848C>A ENSP00000493726.1:n.-77+5848C>A
ENST00000650689.1:n.660+5848C>A
ENST00000651183.1:c.-77+5848C>A ENSP00000498723.1:n.-77+5848C>A
ENST00000297784.9:c.281C>A ENSP00000297784.5:p.Ala94Glu
ENST00000340019.4:c.281C>A ENSP00000341433.3:p.Ala94Glu
NM_138691.2:c.281C>A NP_619636.2:p.Ala94Glu
XM_011518213.1:c.869C>A XP_011516515.1:p.Ala290Glu
XM_017014256.1:c.284C>A XP_016869745.1:p.Ala95Glu
NM_138691.3:c.281C>A MANE Select NP_619636.2:p.Ala94Glu