Canonical Allele Identifier: CA193301051

Gene: TMC1

Linked Data

• dbSNP Id: rs541795877
• gnomAD v2: 9-75406767-C-G
• gnomAD v3: 9-72791851-C-G
• gnomAD v4: 9-72791851-C-G
• MyVariant Identifiers: chr9:g.75406767C>G (hg19) ; chr9:g.72791851C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72791851C>G , CM000671.2:g.72791851C>G	GRCh38
NC_000009.11:g.75406767C>G , CM000671.1:g.75406767C>G	GRCh37
NC_000009.10:g.74596587C>G	NCBI36
NG_008213.1:g.275051C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1225-35C>G MANE Select	ENSP00000297784.6:n.1225-35C>G
ENST00000644967.1:c.787-35C>G	ENSP00000496159.1:n.787-35C>G
ENST00000645053.1:c.787-35C>G	ENSP00000493838.1:n.787-35C>G
ENST00000645208.2:c.1225-35C>G	ENSP00000494684.1:n.1225-35C>G
ENST00000645773.1:c.1099-35C>G	ENSP00000493698.1:n.1099-35C>G
ENST00000645787.1:n.1265-35C>G
ENST00000646619.1:c.787-35C>G	ENSP00000493726.1:n.787-35C>G
ENST00000650689.1:n.1523-35C>G
ENST00000651183.1:c.787-35C>G	ENSP00000498723.1:n.787-35C>G
ENST00000297784.9:c.1225-35C>G	ENSP00000297784.5:n.1225-35C>G
ENST00000340019.4:c.1225-35C>G	ENSP00000341433.3:n.1225-35C>G
NM_138691.2:c.1225-35C>G	NP_619636.2:n.1225-35C>G
XM_011518213.1:c.1813-35C>G	XP_011516515.1:n.1813-35C>G
XM_017014256.1:c.1228-35C>G	XP_016869745.1:n.1228-35C>G
NM_138691.3:c.1225-35C>G MANE Select	NP_619636.2:n.1225-35C>G