Canonical Allele Identifier: CA2147608609
Gene: TTLL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707354_75707356delinsCAT , CM000676.2:g.75707354_75707356delinsCAT GRCh38
NC_000014.8:g.76173697_76173699delinsCAT , CM000676.1:g.76173697_76173699delinsCAT GRCh37
NC_000014.7:g.75243450_75243452delinsCAT NCBI36
NG_016974.1:g.51147_51149delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.655+267_656-267delinsCAT MANE Select ENSP00000298832.9:n.655+267_656-267delinsCAT
ENST00000286650.9:c.655+267_656-267delinsCAT ENSP00000286650.5:n.655+267_656-267delinsCAT
ENST00000298832.13:c.655+267_656-267delinsCAT ENSP00000298832.9:n.655+267_656-267delinsCAT
ENST00000555422.5:n.124+267_125-267delinsCAT
ENST00000556173.5:n.581+267_582-267delinsCAT
ENST00000557636.5:c.655+267_656-267delinsCAT ENSP00000450713.1:n.655+267_656-267delinsCAT
NM_015072.4:c.655+267_656-267delinsCAT NP_055887.3:n.655+267_656-267delinsCAT
NM_015072.5:c.655+267_656-267delinsCAT MANE Select NP_055887.3:n.655+267_656-267delinsCAT