Canonical Allele Identifier: CA373724395
Gene: TMC1 HGNC NCBI

Linked Data

dbSNP Id: rs1826624806
gnomAD v4: 9-72700525-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72700525G>A , CM000671.2:g.72700525G>A GRCh38
NC_000009.11:g.75315441G>A , CM000671.1:g.75315441G>A GRCh37
NC_000009.10:g.74505261G>A NCBI36
NG_008213.1:g.183725G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.244G>A MANE Select ENSP00000297784.6:p.Glu82Lys
ENST00000644967.1:c.-77+5811G>A ENSP00000496159.1:n.-77+5811G>A
ENST00000645053.1:c.-77+5811G>A ENSP00000493838.1:n.-77+5811G>A
ENST00000645208.2:c.244G>A ENSP00000494684.1:p.Glu82Lys
ENST00000645773.1:c.236+5811G>A ENSP00000493698.1:n.236+5811G>A
ENST00000645787.1:n.284G>A
ENST00000646244.1:n.694G>A
ENST00000646619.1:c.-77+5811G>A ENSP00000493726.1:n.-77+5811G>A
ENST00000650689.1:n.660+5811G>A
ENST00000651183.1:c.-77+5811G>A ENSP00000498723.1:n.-77+5811G>A
ENST00000297784.9:c.244G>A ENSP00000297784.5:p.Glu82Lys
ENST00000340019.4:c.244G>A ENSP00000341433.3:p.Glu82Lys
NM_138691.2:c.244G>A NP_619636.2:p.Glu82Lys
XM_011518213.1:c.832G>A XP_011516515.1:p.Glu278Lys
XM_017014256.1:c.247G>A XP_016869745.1:p.Glu83Lys
NM_138691.3:c.244G>A MANE Select NP_619636.2:p.Glu82Lys