Canonical Allele Identifier: CA1855120607

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820761_72820762delinsTG , CM000671.2:g.72820761_72820762delinsTG	GRCh38
NC_000009.11:g.75435677_75435678delinsTG , CM000671.1:g.75435677_75435678delinsTG	GRCh37
NC_000009.10:g.74625497_74625498delinsTG	NCBI36
NG_008213.1:g.303961_303962delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1764-81_1764-80delinsTG MANE Select	ENSP00000297784.6:n.1764-81_1764-80delinsTG
ENST00000644967.1:c.*204-81_*204-80delinsTG	ENSP00000496159.1:n.*204-81_*204-80delinsTG
ENST00000645053.1:c.1258-6108_1258-6107delinsTG	ENSP00000493838.1:n.1258-6108_1258-6107delinsTG
ENST00000645208.2:c.1764-81_1764-80delinsTG	ENSP00000494684.1:n.1764-81_1764-80delinsTG
ENST00000645773.1:c.1638-81_1638-80delinsTG	ENSP00000493698.1:n.1638-81_1638-80delinsTG
ENST00000645787.1:n.1907-81_1907-80delinsTG
ENST00000646619.1:c.1326-81_1326-80delinsTG	ENSP00000493726.1:n.1326-81_1326-80delinsTG
ENST00000651183.1:c.1326-81_1326-80delinsTG	ENSP00000498723.1:n.1326-81_1326-80delinsTG
ENST00000297784.9:c.1764-81_1764-80delinsTG	ENSP00000297784.5:n.1764-81_1764-80delinsTG
ENST00000340019.4:c.1764-81_1764-80delinsTG	ENSP00000341433.3:n.1764-81_1764-80delinsTG
ENST00000469455.1:n.245-81_245-80delinsTG
ENST00000486417.5:n.662-81_662-80delinsTG
NM_138691.2:c.1764-81_1764-80delinsTG	NP_619636.2:n.1764-81_1764-80delinsTG
XM_011518213.1:c.2352-81_2352-80delinsTG	XP_011516515.1:n.2352-81_2352-80delinsTG
XM_017014256.1:c.1767-81_1767-80delinsTG	XP_016869745.1:n.1767-81_1767-80delinsTG
NM_138691.3:c.1764-81_1764-80delinsTG MANE Select	NP_619636.2:n.1764-81_1764-80delinsTG