Canonical Allele Identifier: CA373724608

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75315529G>C (hg19) ; chr9:g.72700613G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72700613G>C , CM000671.2:g.72700613G>C	GRCh38
NC_000009.11:g.75315529G>C , CM000671.1:g.75315529G>C	GRCh37
NC_000009.10:g.74505349G>C	NCBI36
NG_008213.1:g.183813G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.332G>C MANE Select	ENSP00000297784.6:p.Trp111Ser
ENST00000644967.1:c.-77+5899G>C	ENSP00000496159.1:n.-77+5899G>C
ENST00000645053.1:c.-77+5899G>C	ENSP00000493838.1:n.-77+5899G>C
ENST00000645208.2:c.332G>C	ENSP00000494684.1:p.Trp111Ser
ENST00000645773.1:c.236+5899G>C	ENSP00000493698.1:n.236+5899G>C
ENST00000645787.1:n.372G>C
ENST00000646244.1:n.782G>C
ENST00000646619.1:c.-77+5899G>C	ENSP00000493726.1:n.-77+5899G>C
ENST00000650689.1:n.660+5899G>C
ENST00000651183.1:c.-77+5899G>C	ENSP00000498723.1:n.-77+5899G>C
ENST00000297784.9:c.332G>C	ENSP00000297784.5:p.Trp111Ser
ENST00000340019.4:c.332G>C	ENSP00000341433.3:p.Trp111Ser
NM_138691.2:c.332G>C	NP_619636.2:p.Trp111Ser
XM_011518213.1:c.920G>C	XP_011516515.1:p.Trp307Ser
XM_017014256.1:c.335G>C	XP_016869745.1:p.Trp112Ser
NM_138691.3:c.332G>C MANE Select	NP_619636.2:p.Trp111Ser