Canonical Allele Identifier: CA373723707

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75309498G>C (hg19) ; chr9:g.72694582G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72694582G>C , CM000671.2:g.72694582G>C	GRCh38
NC_000009.11:g.75309498G>C , CM000671.1:g.75309498G>C	GRCh37
NC_000009.10:g.74499318G>C	NCBI36
NG_008213.1:g.177782G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000297784.10:c.104G>C MANE Select	ENSP00000297784.6:p.Arg35Thr
ENST00000644967.1:c.-209G>C	ENSP00000496159.1:n.-209G>C
ENST00000645053.1:c.-209G>C	ENSP00000493838.1:n.-209G>C
ENST00000645208.2:c.104G>C	ENSP00000494684.1:p.Arg35Thr
ENST00000645773.1:c.104G>C	ENSP00000493698.1:p.Arg35Thr
ENST00000645787.1:n.144G>C
ENST00000646244.1:n.554G>C
ENST00000646619.1:c.-209G>C	ENSP00000493726.1:n.-209G>C
ENST00000650689.1:n.528G>C
ENST00000651183.1:c.-209G>C	ENSP00000498723.1:n.-209G>C
ENST00000297784.9:c.104G>C	ENSP00000297784.5:p.Arg35Thr
ENST00000340019.4:c.104G>C	ENSP00000341433.3:p.Arg35Thr
NM_138691.2:c.104G>C	NP_619636.2:p.Arg35Thr
XM_011518213.1:c.692G>C	XP_011516515.1:p.Arg231Thr
XM_017014256.1:c.107G>C	XP_016869745.1:p.Arg36Thr
NM_138691.3:c.104G>C MANE Select	NP_619636.2:p.Arg35Thr