Canonical Allele Identifier: CA5081628

Gene: TMC1

Linked Data

• dbSNP Id: rs367859335
• ExAC: 9:75309665 A / G
• gnomAD v2: 9-75309665-A-G
• gnomAD v3: 9-72694749-A-G
• gnomAD v4: 9-72694749-A-G
• MyVariant Identifiers: chr9:g.75309665A>G (hg19) ; chr9:g.72694749A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72694749A>G , CM000671.2:g.72694749A>G	GRCh38
NC_000009.11:g.75309665A>G , CM000671.1:g.75309665A>G	GRCh37
NC_000009.10:g.74499485A>G	NCBI36
NG_008213.1:g.177949A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.236+35A>G MANE Select	ENSP00000297784.6:n.236+35A>G
ENST00000644967.1:c.-77+35A>G	ENSP00000496159.1:n.-77+35A>G
ENST00000645053.1:c.-77+35A>G	ENSP00000493838.1:n.-77+35A>G
ENST00000645208.2:c.236+35A>G	ENSP00000494684.1:n.236+35A>G
ENST00000645773.1:c.236+35A>G	ENSP00000493698.1:n.236+35A>G
ENST00000645787.1:n.276+35A>G
ENST00000646244.1:n.686+35A>G
ENST00000646619.1:c.-77+35A>G	ENSP00000493726.1:n.-77+35A>G
ENST00000650689.1:n.660+35A>G
ENST00000651183.1:c.-77+35A>G	ENSP00000498723.1:n.-77+35A>G
ENST00000297784.9:c.236+35A>G	ENSP00000297784.5:n.236+35A>G
ENST00000340019.4:c.236+35A>G	ENSP00000341433.3:n.236+35A>G
NM_138691.2:c.236+35A>G	NP_619636.2:n.236+35A>G
XM_011518213.1:c.824+35A>G	XP_011516515.1:n.824+35A>G
XM_017014256.1:c.239+35A>G	XP_016869745.1:n.239+35A>G
NM_138691.3:c.236+35A>G MANE Select	NP_619636.2:n.236+35A>G