Canonical Allele Identifier: CA373505702

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75406805A>G (hg19) ; chr9:g.72791889A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72791889A>G , CM000671.2:g.72791889A>G	GRCh38
NC_000009.11:g.75406805A>G , CM000671.1:g.75406805A>G	GRCh37
NC_000009.10:g.74596625A>G	NCBI36
NG_008213.1:g.275089A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1228A>G MANE Select	ENSP00000297784.6:p.Asn410Asp
ENST00000644967.1:c.790A>G	ENSP00000496159.1:p.Asn264Asp
ENST00000645053.1:c.790A>G	ENSP00000493838.1:p.Asn264Asp
ENST00000645208.2:c.1228A>G	ENSP00000494684.1:p.Asn410Asp
ENST00000645773.1:c.1102A>G	ENSP00000493698.1:p.Asn368Asp
ENST00000645787.1:n.1268A>G
ENST00000646619.1:c.790A>G	ENSP00000493726.1:p.Asn264Asp
ENST00000650689.1:n.1526A>G
ENST00000651183.1:c.790A>G	ENSP00000498723.1:p.Asn264Asp
ENST00000297784.9:c.1228A>G	ENSP00000297784.5:p.Asn410Asp
ENST00000340019.4:c.1228A>G	ENSP00000341433.3:p.Asn410Asp
NM_138691.2:c.1228A>G	NP_619636.2:p.Asn410Asp
XM_011518213.1:c.1816A>G	XP_011516515.1:p.Asn606Asp
XM_017014256.1:c.1231A>G	XP_016869745.1:p.Asn411Asp
NM_138691.3:c.1228A>G MANE Select	NP_619636.2:p.Asn410Asp