Canonical Allele Identifier: CA373505885

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75406830T>C (hg19) ; chr9:g.72791914T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72791914T>C , CM000671.2:g.72791914T>C	GRCh38
NC_000009.11:g.75406830T>C , CM000671.1:g.75406830T>C	GRCh37
NC_000009.10:g.74596650T>C	NCBI36
NG_008213.1:g.275114T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1253T>C MANE Select	ENSP00000297784.6:p.Met418Thr
ENST00000644967.1:c.815T>C	ENSP00000496159.1:p.Met272Thr
ENST00000645053.1:c.815T>C	ENSP00000493838.1:p.Met272Thr
ENST00000645208.2:c.1253T>C	ENSP00000494684.1:p.Met418Thr
ENST00000645773.1:c.1127T>C	ENSP00000493698.1:p.Met376Thr
ENST00000645787.1:n.1293T>C
ENST00000646619.1:c.815T>C	ENSP00000493726.1:p.Met272Thr
ENST00000650689.1:n.1551T>C
ENST00000651183.1:c.815T>C	ENSP00000498723.1:p.Met272Thr
ENST00000297784.9:c.1253T>C	ENSP00000297784.5:p.Met418Thr
ENST00000340019.4:c.1253T>C	ENSP00000341433.3:p.Met418Thr
NM_138691.2:c.1253T>C	NP_619636.2:p.Met418Thr
XM_011518213.1:c.1841T>C	XP_011516515.1:p.Met614Thr
XM_017014256.1:c.1256T>C	XP_016869745.1:p.Met419Thr
NM_138691.3:c.1253T>C MANE Select	NP_619636.2:p.Met418Thr