Canonical Allele Identifier: CA2147608697
Gene: TTLL5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707553G= , CM000676.2:g.75707553G= GRCh38
NC_000014.8:g.76173896G= , CM000676.1:g.76173896G= GRCh37
NC_000014.7:g.75243649G= NCBI36
NG_016974.1:g.51346G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298832.14:c.656-70G= MANE Select ENSP00000298832.9:n.656-70G=
ENST00000286650.9:c.656-70G= ENSP00000286650.5:n.656-70G=
ENST00000298832.13:c.656-70G= ENSP00000298832.9:n.656-70G=
ENST00000555422.5:n.125-70G=
ENST00000556173.5:n.582-70G=
ENST00000557636.5:c.656-70G= ENSP00000450713.1:n.656-70G=
NM_015072.4:c.656-70G= NP_055887.3:n.656-70G=
NM_015072.5:c.656-70G= MANE Select NP_055887.3:n.656-70G=
Search 100 bp 5'
Search 100 bp 3'