Canonical Allele Identifier: CA465188584

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75309532A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72694616A>G , CM000671.2:g.72694616A>G	GRCh38
NC_000009.11:g.75309532A>G , CM000671.1:g.75309532A>G	GRCh37
NC_000009.10:g.74499352A>G	NCBI36
NG_008213.1:g.177816A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.138A>G MANE Select	ENSP00000297784.6:p.Arg46=
ENST00000644967.1:c.-175A>G	ENSP00000496159.1:n.-175A>G
ENST00000645053.1:c.-175A>G	ENSP00000493838.1:n.-175A>G
ENST00000645208.2:c.138A>G	ENSP00000494684.1:p.Arg46=
ENST00000645773.1:c.138A>G	ENSP00000493698.1:p.Arg46=
ENST00000645787.1:n.178A>G
ENST00000646244.1:n.588A>G
ENST00000646619.1:c.-175A>G	ENSP00000493726.1:n.-175A>G
ENST00000650689.1:n.562A>G
ENST00000651183.1:c.-175A>G	ENSP00000498723.1:n.-175A>G
ENST00000297784.9:c.138A>G	ENSP00000297784.5:p.Arg46=
ENST00000340019.4:c.138A>G	ENSP00000341433.3:p.Arg46=
NM_138691.2:c.138A>G	NP_619636.2:p.Arg46=
XM_011518213.1:c.726A>G	XP_011516515.1:p.Arg242=
XM_017014256.1:c.141A>G	XP_016869745.1:p.Arg47=
NM_138691.3:c.138A>G MANE Select	NP_619636.2:p.Arg46=