Canonical Allele Identifier: CA708599785
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs1279207957

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707336del , CM000676.2:g.75707336del GRCh38
NC_000014.8:g.76173679del , CM000676.1:g.76173679del GRCh37
NC_000014.7:g.75243432del NCBI36
NG_016974.1:g.51129del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.655+249del MANE Select ENSP00000298832.9:n.655+249del
ENST00000286650.9:c.655+249del ENSP00000286650.5:n.655+249del
ENST00000298832.13:c.655+249del ENSP00000298832.9:n.655+249del
ENST00000555422.5:n.124+249del
ENST00000556173.5:n.581+249del
ENST00000557636.5:c.655+249del ENSP00000450713.1:n.655+249del
NM_015072.4:c.655+249del NP_055887.3:n.655+249del
NM_015072.5:c.655+249del MANE Select NP_055887.3:n.655+249del