Canonical Allele Identifier: CA373670116

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75435925T>C (hg19) ; chr9:g.72821009T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72821009T>C , CM000671.2:g.72821009T>C	GRCh38
NC_000009.11:g.75435925T>C , CM000671.1:g.75435925T>C	GRCh37
NC_000009.10:g.74625745T>C	NCBI36
NG_008213.1:g.304209T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1931T>C MANE Select	ENSP00000297784.6:p.Leu644Pro
ENST00000644967.1:c.*371T>C	ENSP00000496159.1:n.*371T>C
ENST00000645053.1:c.1258-5860T>C	ENSP00000493838.1:n.1258-5860T>C
ENST00000645208.2:c.1931T>C	ENSP00000494684.1:p.Leu644Pro
ENST00000645773.1:c.1805T>C	ENSP00000493698.1:p.Leu602Pro
ENST00000645787.1:n.2074T>C
ENST00000646619.1:c.1493T>C	ENSP00000493726.1:p.Leu498Pro
ENST00000651183.1:c.1493T>C	ENSP00000498723.1:p.Leu498Pro
ENST00000297784.9:c.1931T>C	ENSP00000297784.5:p.Leu644Pro
ENST00000340019.4:c.1931T>C	ENSP00000341433.3:p.Leu644Pro
ENST00000469455.1:n.412T>C
ENST00000486417.5:n.829T>C
NM_138691.2:c.1931T>C	NP_619636.2:p.Leu644Pro
XM_011518213.1:c.2519T>C	XP_011516515.1:p.Leu840Pro
XM_017014256.1:c.1934T>C	XP_016869745.1:p.Leu645Pro
NM_138691.3:c.1931T>C MANE Select	NP_619636.2:p.Leu644Pro