Canonical Allele Identifier: CA373669773

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75435871T>A (hg19) ; chr9:g.72820955T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820955T>A , CM000671.2:g.72820955T>A	GRCh38
NC_000009.11:g.75435871T>A , CM000671.1:g.75435871T>A	GRCh37
NC_000009.10:g.74625691T>A	NCBI36
NG_008213.1:g.304155T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1877T>A MANE Select	ENSP00000297784.6:p.Val626Asp
ENST00000644967.1:c.*317T>A	ENSP00000496159.1:n.*317T>A
ENST00000645053.1:c.1258-5914T>A	ENSP00000493838.1:n.1258-5914T>A
ENST00000645208.2:c.1877T>A	ENSP00000494684.1:p.Val626Asp
ENST00000645773.1:c.1751T>A	ENSP00000493698.1:p.Val584Asp
ENST00000645787.1:n.2020T>A
ENST00000646619.1:c.1439T>A	ENSP00000493726.1:p.Val480Asp
ENST00000651183.1:c.1439T>A	ENSP00000498723.1:p.Val480Asp
ENST00000297784.9:c.1877T>A	ENSP00000297784.5:p.Val626Asp
ENST00000340019.4:c.1877T>A	ENSP00000341433.3:p.Val626Asp
ENST00000469455.1:n.358T>A
ENST00000486417.5:n.775T>A
NM_138691.2:c.1877T>A	NP_619636.2:p.Val626Asp
XM_011518213.1:c.2465T>A	XP_011516515.1:p.Val822Asp
XM_017014256.1:c.1880T>A	XP_016869745.1:p.Val627Asp
NM_138691.3:c.1877T>A MANE Select	NP_619636.2:p.Val626Asp