Canonical Allele Identifier: CA1855065588
Gene: TMC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72694854_72694858delinsCTTAA , CM000671.2:g.72694854_72694858delinsCTTAA GRCh38
NC_000009.11:g.75309770_75309774delinsCTTAA , CM000671.1:g.75309770_75309774delinsCTTAA GRCh37
NC_000009.10:g.74499590_74499594delinsCTTAA NCBI36
NG_008213.1:g.178054_178058delinsCTTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.236+140_236+144delinsCTTAA MANE Select ENSP00000297784.6:n.236+140_236+144delinsCTTAA
ENST00000644967.1:c.-77+140_-77+144delinsCTTAA ENSP00000496159.1:n.-77+140_-77+144delinsCTTAA
ENST00000645053.1:c.-77+140_-77+144delinsCTTAA ENSP00000493838.1:n.-77+140_-77+144delinsCTTAA
ENST00000645208.2:c.236+140_236+144delinsCTTAA ENSP00000494684.1:n.236+140_236+144delinsCTTAA
ENST00000645773.1:c.236+140_236+144delinsCTTAA ENSP00000493698.1:n.236+140_236+144delinsCTTAA
ENST00000645787.1:n.276+140_276+144delinsCTTAA
ENST00000646244.1:n.686+140_686+144delinsCTTAA
ENST00000646619.1:c.-77+140_-77+144delinsCTTAA ENSP00000493726.1:n.-77+140_-77+144delinsCTTAA
ENST00000650689.1:n.660+140_660+144delinsCTTAA
ENST00000651183.1:c.-77+140_-77+144delinsCTTAA ENSP00000498723.1:n.-77+140_-77+144delinsCTTAA
ENST00000297784.9:c.236+140_236+144delinsCTTAA ENSP00000297784.5:n.236+140_236+144delinsCTTAA
ENST00000340019.4:c.236+140_236+144delinsCTTAA ENSP00000341433.3:n.236+140_236+144delinsCTTAA
NM_138691.2:c.236+140_236+144delinsCTTAA NP_619636.2:n.236+140_236+144delinsCTTAA
XM_011518213.1:c.824+140_824+144delinsCTTAA XP_011516515.1:n.824+140_824+144delinsCTTAA
XM_017014256.1:c.239+140_239+144delinsCTTAA XP_016869745.1:n.239+140_239+144delinsCTTAA
NM_138691.3:c.236+140_236+144delinsCTTAA MANE Select NP_619636.2:n.236+140_236+144delinsCTTAA