Canonical Allele Identifier: CA588441068

Gene: TMC1

Linked Data

• dbSNP Id: rs1340587729
• gnomAD v2: 9-75431174-G-T
• gnomAD v4: 9-72816258-G-T
• MyVariant Identifiers: chr9:g.75431174G>T (hg19) ; chr9:g.72816258G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816258G>T , CM000671.2:g.72816258G>T	GRCh38
NC_000009.11:g.75431174G>T , CM000671.1:g.75431174G>T	GRCh37
NC_000009.10:g.74620994G>T	NCBI36
NG_008213.1:g.299458G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1763+48G>T MANE Select	ENSP00000297784.6:n.1763+48G>T
ENST00000644967.1:c.1325+48G>T	ENSP00000496159.1:n.1325+48G>T
ENST00000645053.1:c.1258-10611G>T	ENSP00000493838.1:n.1258-10611G>T
ENST00000645208.2:c.1763+48G>T	ENSP00000494684.1:n.1763+48G>T
ENST00000645773.1:c.1637+48G>T	ENSP00000493698.1:n.1637+48G>T
ENST00000645787.1:n.1906+48G>T
ENST00000646619.1:c.1325+48G>T	ENSP00000493726.1:n.1325+48G>T
ENST00000651183.1:c.1325+48G>T	ENSP00000498723.1:n.1325+48G>T
ENST00000297784.9:c.1763+48G>T	ENSP00000297784.5:n.1763+48G>T
ENST00000340019.4:c.1763+48G>T	ENSP00000341433.3:n.1763+48G>T
ENST00000469455.1:n.244+48G>T
ENST00000486417.5:n.387+48G>T
NM_138691.2:c.1763+48G>T	NP_619636.2:n.1763+48G>T
XM_011518213.1:c.2351+48G>T	XP_011516515.1:n.2351+48G>T
XM_017014256.1:c.1766+48G>T	XP_016869745.1:n.1766+48G>T
NM_138691.3:c.1763+48G>T MANE Select	NP_619636.2:n.1763+48G>T