Canonical Allele Identifier: CA31904265
Gene: TMCO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165753968del , CM000663.2:g.165753968del GRCh38
NC_000001.10:g.165723205del , CM000663.1:g.165723205del GRCh37
NC_000001.9:g.163989829del NCBI36
NG_032004.1:g.19956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367881.11:c.255+261del MANE Select ENSP00000356856.6:n.255+261del
ENST00000465705.4:c.*86+261del ENSP00000463105.2:n.*86+261del
ENST00000476143.7:c.*45+261del ENSP00000464127.2:n.*45+261del
ENST00000367881.9:c.408+261del ENSP00000356856.5:n.408+261del
ENST00000392129.10:c.255+261del ENSP00000375975.5:n.255+261del
ENST00000464650.5:c.3+261del ENSP00000463951.1:n.3+261del
ENST00000465705.3:c.*86+261del ENSP00000463105.1:n.*86+261del
ENST00000476143.6:c.332+261del
ENST00000481278.5:c.219+261del ENSP00000462300.1:n.219+261del
ENST00000580248.5:c.3+261del ENSP00000462588.1:n.3+261del
ENST00000612311.4:c.408+261del ENSP00000480514.1:n.408+261del
NM_001256164.1:c.306+261del NP_001243093.1:n.306+261del
NM_001256165.1:c.219+261del NP_001243094.1:n.219+261del
NM_019026.4:c.408+261del NP_061899.2:n.408+261del
NR_045818.1:n.349+261del
NM_001366129.1:c.255+261del NP_001353058.1:n.255+261del
NM_019026.5:c.255+261del NP_061899.3:n.255+261del
NM_019026.6:c.255+261del MANE Select NP_061899.3:n.255+261del