Canonical Allele Identifier: CA373505108

Gene: TMC1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72789303T>A , CM000671.2:g.72789303T>A	GRCh38
NC_000009.11:g.75404219T>A , CM000671.1:g.75404219T>A	GRCh37
NC_000009.10:g.74594039T>A	NCBI36
NG_008213.1:g.272503T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1210T>A MANE Select	ENSP00000297784.6:p.Trp404Arg
ENST00000644967.1:c.772T>A	ENSP00000496159.1:p.Trp258Arg
ENST00000645053.1:c.772T>A	ENSP00000493838.1:p.Trp258Arg
ENST00000645208.2:c.1210T>A	ENSP00000494684.1:p.Trp404Arg
ENST00000645773.1:c.1084T>A	ENSP00000493698.1:p.Trp362Arg
ENST00000645787.1:n.1250T>A
ENST00000646619.1:c.772T>A	ENSP00000493726.1:p.Trp258Arg
ENST00000650689.1:n.1508T>A
ENST00000651183.1:c.772T>A	ENSP00000498723.1:p.Trp258Arg
ENST00000297784.9:c.1210T>A	ENSP00000297784.5:p.Trp404Arg
ENST00000340019.4:c.1210T>A	ENSP00000341433.3:p.Trp404Arg
NM_138691.2:c.1210T>A	NP_619636.2:p.Trp404Arg
XM_011518213.1:c.1798T>A	XP_011516515.1:p.Trp600Arg
XM_017014256.1:c.1213T>A	XP_016869745.1:p.Trp405Arg
NM_138691.3:c.1210T>A MANE Select	NP_619636.2:p.Trp404Arg