Canonical Allele Identifier: CA373668474

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75431121G>T (hg19) ; chr9:g.72816205G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816205G>T , CM000671.2:g.72816205G>T	GRCh38
NC_000009.11:g.75431121G>T , CM000671.1:g.75431121G>T	GRCh37
NC_000009.10:g.74620941G>T	NCBI36
NG_008213.1:g.299405G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1758G>T MANE Select	ENSP00000297784.6:p.Met586Ile
ENST00000644967.1:c.1320G>T	ENSP00000496159.1:p.Met440Ile
ENST00000645053.1:c.1258-10664G>T	ENSP00000493838.1:n.1258-10664G>T
ENST00000645208.2:c.1758G>T	ENSP00000494684.1:p.Met586Ile
ENST00000645773.1:c.1632G>T	ENSP00000493698.1:p.Met544Ile
ENST00000645787.1:n.1901G>T
ENST00000646619.1:c.1320G>T	ENSP00000493726.1:p.Met440Ile
ENST00000651183.1:c.1320G>T	ENSP00000498723.1:p.Met440Ile
ENST00000297784.9:c.1758G>T	ENSP00000297784.5:p.Met586Ile
ENST00000340019.4:c.1758G>T	ENSP00000341433.3:p.Met586Ile
ENST00000469455.1:n.239G>T
ENST00000486417.5:n.382G>T
NM_138691.2:c.1758G>T	NP_619636.2:p.Met586Ile
XM_011518213.1:c.2346G>T	XP_011516515.1:p.Met782Ile
XM_017014256.1:c.1761G>T	XP_016869745.1:p.Met587Ile
NM_138691.3:c.1758G>T MANE Select	NP_619636.2:p.Met586Ile