Canonical Allele Identifier: CA1855120754

Gene: TMC1

Linked Data

• dbSNP Id: rs1828864806
• gnomAD v3: 9-72821086-C-G
• gnomAD v4: 9-72821086-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72821086C>G , CM000671.2:g.72821086C>G	GRCh38
NC_000009.11:g.75436002C>G , CM000671.1:g.75436002C>G	GRCh37
NC_000009.10:g.74625822C>G	NCBI36
NG_008213.1:g.304286C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.2003+5C>G MANE Select	ENSP00000297784.6:n.2003+5C>G
ENST00000644967.1:c.*443+5C>G	ENSP00000496159.1:n.*443+5C>G
ENST00000645053.1:c.1258-5783C>G	ENSP00000493838.1:n.1258-5783C>G
ENST00000645208.2:c.2003+5C>G	ENSP00000494684.1:n.2003+5C>G
ENST00000645773.1:c.1877+5C>G	ENSP00000493698.1:n.1877+5C>G
ENST00000645787.1:n.2146+5C>G
ENST00000646619.1:c.1565+5C>G	ENSP00000493726.1:n.1565+5C>G
ENST00000651183.1:c.1565+5C>G	ENSP00000498723.1:n.1565+5C>G
ENST00000297784.9:c.2003+5C>G	ENSP00000297784.5:n.2003+5C>G
ENST00000340019.4:c.2003+5C>G	ENSP00000341433.3:n.2003+5C>G
ENST00000469455.1:n.484+5C>G
ENST00000486417.5:n.901+5C>G
NM_138691.2:c.2003+5C>G	NP_619636.2:n.2003+5C>G
XM_011518213.1:c.2591+5C>G	XP_011516515.1:n.2591+5C>G
XM_017014256.1:c.2006+5C>G	XP_016869745.1:n.2006+5C>G
NM_138691.3:c.2003+5C>G MANE Select	NP_619636.2:n.2003+5C>G