Canonical Allele Identifier: CA373668400

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75431105T>A (hg19) ; chr9:g.72816189T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816189T>A , CM000671.2:g.72816189T>A	GRCh38
NC_000009.11:g.75431105T>A , CM000671.1:g.75431105T>A	GRCh37
NC_000009.10:g.74620925T>A	NCBI36
NG_008213.1:g.299389T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1742T>A MANE Select	ENSP00000297784.6:p.Ile581Asn
ENST00000644967.1:c.1304T>A	ENSP00000496159.1:p.Ile435Asn
ENST00000645053.1:c.1258-10680T>A	ENSP00000493838.1:n.1258-10680T>A
ENST00000645208.2:c.1742T>A	ENSP00000494684.1:p.Ile581Asn
ENST00000645773.1:c.1616T>A	ENSP00000493698.1:p.Ile539Asn
ENST00000645787.1:n.1885T>A
ENST00000646619.1:c.1304T>A	ENSP00000493726.1:p.Ile435Asn
ENST00000651183.1:c.1304T>A	ENSP00000498723.1:p.Ile435Asn
ENST00000297784.9:c.1742T>A	ENSP00000297784.5:p.Ile581Asn
ENST00000340019.4:c.1742T>A	ENSP00000341433.3:p.Ile581Asn
ENST00000469455.1:n.223T>A
ENST00000486417.5:n.366T>A
NM_138691.2:c.1742T>A	NP_619636.2:p.Ile581Asn
XM_011518213.1:c.2330T>A	XP_011516515.1:p.Ile777Asn
XM_017014256.1:c.1745T>A	XP_016869745.1:p.Ile582Asn
NM_138691.3:c.1742T>A MANE Select	NP_619636.2:p.Ile581Asn