Canonical Allele Identifier: CA373723968

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75309612G>T (hg19) ; chr9:g.72694696G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72694696G>T , CM000671.2:g.72694696G>T	GRCh38
NC_000009.11:g.75309612G>T , CM000671.1:g.75309612G>T	GRCh37
NC_000009.10:g.74499432G>T	NCBI36
NG_008213.1:g.177896G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.218G>T MANE Select	ENSP00000297784.6:p.Arg73Met
ENST00000644967.1:c.-95G>T	ENSP00000496159.1:n.-95G>T
ENST00000645053.1:c.-95G>T	ENSP00000493838.1:n.-95G>T
ENST00000645208.2:c.218G>T	ENSP00000494684.1:p.Arg73Met
ENST00000645773.1:c.218G>T	ENSP00000493698.1:p.Arg73Met
ENST00000645787.1:n.258G>T
ENST00000646244.1:n.668G>T
ENST00000646619.1:c.-95G>T	ENSP00000493726.1:n.-95G>T
ENST00000650689.1:n.642G>T
ENST00000651183.1:c.-95G>T	ENSP00000498723.1:n.-95G>T
ENST00000297784.9:c.218G>T	ENSP00000297784.5:p.Arg73Met
ENST00000340019.4:c.218G>T	ENSP00000341433.3:p.Arg73Met
NM_138691.2:c.218G>T	NP_619636.2:p.Arg73Met
XM_011518213.1:c.806G>T	XP_011516515.1:p.Arg269Met
XM_017014256.1:c.221G>T	XP_016869745.1:p.Arg74Met
NM_138691.3:c.218G>T MANE Select	NP_619636.2:p.Arg73Met