Canonical Allele Identifier: CA2730163927
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs2140172590

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707391A>G , CM000676.2:g.75707391A>G GRCh38
NC_000014.8:g.76173734A>G , CM000676.1:g.76173734A>G GRCh37
NC_000014.7:g.75243487A>G NCBI36
NG_016974.1:g.51184A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.656-232A>G MANE Select ENSP00000298832.9:n.656-232A>G
ENST00000286650.9:c.656-232A>G ENSP00000286650.5:n.656-232A>G
ENST00000298832.13:c.656-232A>G ENSP00000298832.9:n.656-232A>G
ENST00000555422.5:n.125-232A>G
ENST00000556173.5:n.582-232A>G
ENST00000557636.5:c.656-232A>G ENSP00000450713.1:n.656-232A>G
NM_015072.4:c.656-232A>G NP_055887.3:n.656-232A>G
NM_015072.5:c.656-232A>G MANE Select NP_055887.3:n.656-232A>G