Canonical Allele Identifier: CA373724511

Gene: TMC1

Linked Data

• gnomAD v4: 9-72700571-A-T
• MyVariant Identifiers: chr9:g.75315487A>T (hg19) ; chr9:g.72700571A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72700571A>T , CM000671.2:g.72700571A>T	GRCh38
NC_000009.11:g.75315487A>T , CM000671.1:g.75315487A>T	GRCh37
NC_000009.10:g.74505307A>T	NCBI36
NG_008213.1:g.183771A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.290A>T MANE Select	ENSP00000297784.6:p.Asp97Val
ENST00000644967.1:c.-77+5857A>T	ENSP00000496159.1:n.-77+5857A>T
ENST00000645053.1:c.-77+5857A>T	ENSP00000493838.1:n.-77+5857A>T
ENST00000645208.2:c.290A>T	ENSP00000494684.1:p.Asp97Val
ENST00000645773.1:c.236+5857A>T	ENSP00000493698.1:n.236+5857A>T
ENST00000645787.1:n.330A>T
ENST00000646244.1:n.740A>T
ENST00000646619.1:c.-77+5857A>T	ENSP00000493726.1:n.-77+5857A>T
ENST00000650689.1:n.660+5857A>T
ENST00000651183.1:c.-77+5857A>T	ENSP00000498723.1:n.-77+5857A>T
ENST00000297784.9:c.290A>T	ENSP00000297784.5:p.Asp97Val
ENST00000340019.4:c.290A>T	ENSP00000341433.3:p.Asp97Val
NM_138691.2:c.290A>T	NP_619636.2:p.Asp97Val
XM_011518213.1:c.878A>T	XP_011516515.1:p.Asp293Val
XM_017014256.1:c.293A>T	XP_016869745.1:p.Asp98Val
NM_138691.3:c.290A>T MANE Select	NP_619636.2:p.Asp97Val