Canonical Allele Identifier: CA2579354236

Gene: TMC1

Linked Data

• gnomAD v4: 9-72791845-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72791845A>T , CM000671.2:g.72791845A>T	GRCh38
NC_000009.11:g.75406761A>T , CM000671.1:g.75406761A>T	GRCh37
NC_000009.10:g.74596581A>T	NCBI36
NG_008213.1:g.275045A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1225-41A>T MANE Select	ENSP00000297784.6:n.1225-41A>T
ENST00000644967.1:c.787-41A>T	ENSP00000496159.1:n.787-41A>T
ENST00000645053.1:c.787-41A>T	ENSP00000493838.1:n.787-41A>T
ENST00000645208.2:c.1225-41A>T	ENSP00000494684.1:n.1225-41A>T
ENST00000645773.1:c.1099-41A>T	ENSP00000493698.1:n.1099-41A>T
ENST00000645787.1:n.1265-41A>T
ENST00000646619.1:c.787-41A>T	ENSP00000493726.1:n.787-41A>T
ENST00000650689.1:n.1523-41A>T
ENST00000651183.1:c.787-41A>T	ENSP00000498723.1:n.787-41A>T
ENST00000297784.9:c.1225-41A>T	ENSP00000297784.5:n.1225-41A>T
ENST00000340019.4:c.1225-41A>T	ENSP00000341433.3:n.1225-41A>T
NM_138691.2:c.1225-41A>T	NP_619636.2:n.1225-41A>T
XM_011518213.1:c.1813-41A>T	XP_011516515.1:n.1813-41A>T
XM_017014256.1:c.1228-41A>T	XP_016869745.1:n.1228-41A>T
NM_138691.3:c.1225-41A>T MANE Select	NP_619636.2:n.1225-41A>T