Canonical Allele Identifier: CA465189399

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75315503A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72700587A>C , CM000671.2:g.72700587A>C	GRCh38
NC_000009.11:g.75315503A>C , CM000671.1:g.75315503A>C	GRCh37
NC_000009.10:g.74505323A>C	NCBI36
NG_008213.1:g.183787A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.306A>C MANE Select	ENSP00000297784.6:p.Ile102=
ENST00000644967.1:c.-77+5873A>C	ENSP00000496159.1:n.-77+5873A>C
ENST00000645053.1:c.-77+5873A>C	ENSP00000493838.1:n.-77+5873A>C
ENST00000645208.2:c.306A>C	ENSP00000494684.1:p.Ile102=
ENST00000645773.1:c.236+5873A>C	ENSP00000493698.1:n.236+5873A>C
ENST00000645787.1:n.346A>C
ENST00000646244.1:n.756A>C
ENST00000646619.1:c.-77+5873A>C	ENSP00000493726.1:n.-77+5873A>C
ENST00000650689.1:n.660+5873A>C
ENST00000651183.1:c.-77+5873A>C	ENSP00000498723.1:n.-77+5873A>C
ENST00000297784.9:c.306A>C	ENSP00000297784.5:p.Ile102=
ENST00000340019.4:c.306A>C	ENSP00000341433.3:p.Ile102=
NM_138691.2:c.306A>C	NP_619636.2:p.Ile102=
XM_011518213.1:c.894A>C	XP_011516515.1:p.Ile298=
XM_017014256.1:c.309A>C	XP_016869745.1:p.Ile103=
NM_138691.3:c.306A>C MANE Select	NP_619636.2:p.Ile102=