Canonical Allele Identifier: CA373669615

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75435799T>A (hg19) ; chr9:g.72820883T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820883T>A , CM000671.2:g.72820883T>A	GRCh38
NC_000009.11:g.75435799T>A , CM000671.1:g.75435799T>A	GRCh37
NC_000009.10:g.74625619T>A	NCBI36
NG_008213.1:g.304083T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1805T>A MANE Select	ENSP00000297784.6:p.Ile602Asn
ENST00000644967.1:c.*245T>A	ENSP00000496159.1:n.*245T>A
ENST00000645053.1:c.1258-5986T>A	ENSP00000493838.1:n.1258-5986T>A
ENST00000645208.2:c.1805T>A	ENSP00000494684.1:p.Ile602Asn
ENST00000645773.1:c.1679T>A	ENSP00000493698.1:p.Ile560Asn
ENST00000645787.1:n.1948T>A
ENST00000646619.1:c.1367T>A	ENSP00000493726.1:p.Ile456Asn
ENST00000651183.1:c.1367T>A	ENSP00000498723.1:p.Ile456Asn
ENST00000297784.9:c.1805T>A	ENSP00000297784.5:p.Ile602Asn
ENST00000340019.4:c.1805T>A	ENSP00000341433.3:p.Ile602Asn
ENST00000469455.1:n.286T>A
ENST00000486417.5:n.703T>A
NM_138691.2:c.1805T>A	NP_619636.2:p.Ile602Asn
XM_011518213.1:c.2393T>A	XP_011516515.1:p.Ile798Asn
XM_017014256.1:c.1808T>A	XP_016869745.1:p.Ile603Asn
NM_138691.3:c.1805T>A MANE Select	NP_619636.2:p.Ile602Asn