Canonical Allele Identifier: CA866640417

Gene: TMC1

Linked Data

• dbSNP Id: rs1216998297
• MyVariant Identifiers: chr9:g.75436163A>G (hg19) ; chr9:g.72821247A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72821247A>G , CM000671.2:g.72821247A>G	GRCh38
NC_000009.11:g.75436163A>G , CM000671.1:g.75436163A>G	GRCh37
NC_000009.10:g.74625983A>G	NCBI36
NG_008213.1:g.304447A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.2003+166A>G MANE Select	ENSP00000297784.6:n.2003+166A>G
ENST00000644967.1:c.*443+166A>G	ENSP00000496159.1:n.*443+166A>G
ENST00000645053.1:c.1258-5622A>G	ENSP00000493838.1:n.1258-5622A>G
ENST00000645208.2:c.2003+166A>G	ENSP00000494684.1:n.2003+166A>G
ENST00000645773.1:c.1877+166A>G	ENSP00000493698.1:n.1877+166A>G
ENST00000645787.1:n.2146+166A>G
ENST00000646619.1:c.1565+166A>G	ENSP00000493726.1:n.1565+166A>G
ENST00000651183.1:c.1565+166A>G	ENSP00000498723.1:n.1565+166A>G
ENST00000297784.9:c.2003+166A>G	ENSP00000297784.5:n.2003+166A>G
ENST00000340019.4:c.2003+166A>G	ENSP00000341433.3:n.2003+166A>G
ENST00000469455.1:n.484+166A>G
ENST00000486417.5:n.901+166A>G
NM_138691.2:c.2003+166A>G	NP_619636.2:n.2003+166A>G
XM_011518213.1:c.2591+166A>G	XP_011516515.1:n.2591+166A>G
XM_017014256.1:c.2006+166A>G	XP_016869745.1:n.2006+166A>G
NM_138691.3:c.2003+166A>G MANE Select	NP_619636.2:n.2003+166A>G