Canonical Allele Identifier: CA2697557767

Gene: TMC1

Linked Data

• ClinVar Variation Id: 2768702
• ClinVar RCV Id: RCV003576502

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820827C>G , CM000671.2:g.72820827C>G	GRCh38
NC_000009.11:g.75435743C>G , CM000671.1:g.75435743C>G	GRCh37
NC_000009.10:g.74625563C>G	NCBI36
NG_008213.1:g.304027C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1764-15C>G MANE Select	ENSP00000297784.6:n.1764-15C>G
ENST00000644967.1:c.*204-15C>G	ENSP00000496159.1:n.*204-15C>G
ENST00000645053.1:c.1258-6042C>G	ENSP00000493838.1:n.1258-6042C>G
ENST00000645208.2:c.1764-15C>G	ENSP00000494684.1:n.1764-15C>G
ENST00000645773.1:c.1638-15C>G	ENSP00000493698.1:n.1638-15C>G
ENST00000645787.1:n.1907-15C>G
ENST00000646619.1:c.1326-15C>G	ENSP00000493726.1:n.1326-15C>G
ENST00000651183.1:c.1326-15C>G	ENSP00000498723.1:n.1326-15C>G
ENST00000297784.9:c.1764-15C>G	ENSP00000297784.5:n.1764-15C>G
ENST00000340019.4:c.1764-15C>G	ENSP00000341433.3:n.1764-15C>G
ENST00000469455.1:n.245-15C>G
ENST00000486417.5:n.662-15C>G
NM_138691.2:c.1764-15C>G	NP_619636.2:n.1764-15C>G
XM_011518213.1:c.2352-15C>G	XP_011516515.1:n.2352-15C>G
XM_017014256.1:c.1767-15C>G	XP_016869745.1:n.1767-15C>G
NM_138691.3:c.1764-15C>G MANE Select	NP_619636.2:n.1764-15C>G