Canonical Allele Identifier: CA373668200

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75431060C>G (hg19) ; chr9:g.72816144C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816144C>G , CM000671.2:g.72816144C>G	GRCh38
NC_000009.11:g.75431060C>G , CM000671.1:g.75431060C>G	GRCh37
NC_000009.10:g.74620880C>G	NCBI36
NG_008213.1:g.299344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1697C>G MANE Select	ENSP00000297784.6:p.Pro566Arg
ENST00000644967.1:c.1259C>G	ENSP00000496159.1:p.Pro420Arg
ENST00000645053.1:c.1257+10634C>G	ENSP00000493838.1:n.1257+10634C>G
ENST00000645208.2:c.1697C>G	ENSP00000494684.1:p.Pro566Arg
ENST00000645773.1:c.1571C>G	ENSP00000493698.1:p.Pro524Arg
ENST00000645787.1:n.1840C>G
ENST00000646619.1:c.1259C>G	ENSP00000493726.1:p.Pro420Arg
ENST00000651183.1:c.1259C>G	ENSP00000498723.1:p.Pro420Arg
ENST00000297784.9:c.1697C>G	ENSP00000297784.5:p.Pro566Arg
ENST00000340019.4:c.1697C>G	ENSP00000341433.3:p.Pro566Arg
ENST00000469455.1:n.178C>G
ENST00000486417.5:n.321C>G
NM_138691.2:c.1697C>G	NP_619636.2:p.Pro566Arg
XM_011518213.1:c.2285C>G	XP_011516515.1:p.Pro762Arg
XM_017014256.1:c.1700C>G	XP_016869745.1:p.Pro567Arg
NM_138691.3:c.1697C>G MANE Select	NP_619636.2:p.Pro566Arg