Canonical Allele Identifier: CA465492656

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75435860T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820944T>C , CM000671.2:g.72820944T>C	GRCh38
NC_000009.11:g.75435860T>C , CM000671.1:g.75435860T>C	GRCh37
NC_000009.10:g.74625680T>C	NCBI36
NG_008213.1:g.304144T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1866T>C MANE Select	ENSP00000297784.6:p.Pro622=
ENST00000644967.1:c.*306T>C	ENSP00000496159.1:n.*306T>C
ENST00000645053.1:c.1258-5925T>C	ENSP00000493838.1:n.1258-5925T>C
ENST00000645208.2:c.1866T>C	ENSP00000494684.1:p.Pro622=
ENST00000645773.1:c.1740T>C	ENSP00000493698.1:p.Pro580=
ENST00000645787.1:n.2009T>C
ENST00000646619.1:c.1428T>C	ENSP00000493726.1:p.Pro476=
ENST00000651183.1:c.1428T>C	ENSP00000498723.1:p.Pro476=
ENST00000297784.9:c.1866T>C	ENSP00000297784.5:p.Pro622=
ENST00000340019.4:c.1866T>C	ENSP00000341433.3:p.Pro622=
ENST00000469455.1:n.347T>C
ENST00000486417.5:n.764T>C
NM_138691.2:c.1866T>C	NP_619636.2:p.Pro622=
XM_011518213.1:c.2454T>C	XP_011516515.1:p.Pro818=
XM_017014256.1:c.1869T>C	XP_016869745.1:p.Pro623=
NM_138691.3:c.1866T>C MANE Select	NP_619636.2:p.Pro622=