Canonical Allele Identifier: CA2690286378

Gene: TMC1

Linked Data

• gnomAD v4: 9-72700681-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72700681T>C , CM000671.2:g.72700681T>C	GRCh38
NC_000009.11:g.75315597T>C , CM000671.1:g.75315597T>C	GRCh37
NC_000009.10:g.74505417T>C	NCBI36
NG_008213.1:g.183881T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.362+38T>C MANE Select	ENSP00000297784.6:n.362+38T>C
ENST00000644967.1:c.-77+5967T>C	ENSP00000496159.1:n.-77+5967T>C
ENST00000645053.1:c.-77+5967T>C	ENSP00000493838.1:n.-77+5967T>C
ENST00000645208.2:c.362+38T>C	ENSP00000494684.1:n.362+38T>C
ENST00000645773.1:c.236+5967T>C	ENSP00000493698.1:n.236+5967T>C
ENST00000645787.1:n.402+38T>C
ENST00000646244.1:n.850T>C
ENST00000646619.1:c.-77+5967T>C	ENSP00000493726.1:n.-77+5967T>C
ENST00000650689.1:n.660+5967T>C
ENST00000651183.1:c.-77+5967T>C	ENSP00000498723.1:n.-77+5967T>C
ENST00000297784.9:c.362+38T>C	ENSP00000297784.5:n.362+38T>C
ENST00000340019.4:c.362+38T>C	ENSP00000341433.3:n.362+38T>C
NM_138691.2:c.362+38T>C	NP_619636.2:n.362+38T>C
XM_011518213.1:c.950+38T>C	XP_011516515.1:n.950+38T>C
XM_017014256.1:c.365+38T>C	XP_016869745.1:n.365+38T>C
NM_138691.3:c.362+38T>C MANE Select	NP_619636.2:n.362+38T>C