Canonical Allele Identifier: CA2147608600
Gene: TTLL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707335_75707336delinsTA , CM000676.2:g.75707335_75707336delinsTA GRCh38
NC_000014.8:g.76173678_76173679delinsTA , CM000676.1:g.76173678_76173679delinsTA GRCh37
NC_000014.7:g.75243431_75243432delinsTA NCBI36
NG_016974.1:g.51128_51129delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.655+248_655+249delinsTA MANE Select ENSP00000298832.9:n.655+248_655+249delinsTA
ENST00000286650.9:c.655+248_655+249delinsTA ENSP00000286650.5:n.655+248_655+249delinsTA
ENST00000298832.13:c.655+248_655+249delinsTA ENSP00000298832.9:n.655+248_655+249delinsTA
ENST00000555422.5:n.124+248_124+249delinsTA
ENST00000556173.5:n.581+248_581+249delinsTA
ENST00000557636.5:c.655+248_655+249delinsTA ENSP00000450713.1:n.655+248_655+249delinsTA
NM_015072.4:c.655+248_655+249delinsTA NP_055887.3:n.655+248_655+249delinsTA
NM_015072.5:c.655+248_655+249delinsTA MANE Select NP_055887.3:n.655+248_655+249delinsTA