Canonical Allele Identifier: CA465492701

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75435899C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820983C>T , CM000671.2:g.72820983C>T	GRCh38
NC_000009.11:g.75435899C>T , CM000671.1:g.75435899C>T	GRCh37
NC_000009.10:g.74625719C>T	NCBI36
NG_008213.1:g.304183C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1905C>T MANE Select	ENSP00000297784.6:p.Phe635=
ENST00000644967.1:c.*345C>T	ENSP00000496159.1:n.*345C>T
ENST00000645053.1:c.1258-5886C>T	ENSP00000493838.1:n.1258-5886C>T
ENST00000645208.2:c.1905C>T	ENSP00000494684.1:p.Phe635=
ENST00000645773.1:c.1779C>T	ENSP00000493698.1:p.Phe593=
ENST00000645787.1:n.2048C>T
ENST00000646619.1:c.1467C>T	ENSP00000493726.1:p.Phe489=
ENST00000651183.1:c.1467C>T	ENSP00000498723.1:p.Phe489=
ENST00000297784.9:c.1905C>T	ENSP00000297784.5:p.Phe635=
ENST00000340019.4:c.1905C>T	ENSP00000341433.3:p.Phe635=
ENST00000469455.1:n.386C>T
ENST00000486417.5:n.803C>T
NM_138691.2:c.1905C>T	NP_619636.2:p.Phe635=
XM_011518213.1:c.2493C>T	XP_011516515.1:p.Phe831=
XM_017014256.1:c.1908C>T	XP_016869745.1:p.Phe636=
NM_138691.3:c.1905C>T MANE Select	NP_619636.2:p.Phe635=