Canonical Allele Identifier: CA2147608621
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs1886730857
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707389G>A , CM000676.2:g.75707389G>A GRCh38
NC_000014.8:g.76173732G>A , CM000676.1:g.76173732G>A GRCh37
NC_000014.7:g.75243485G>A NCBI36
NG_016974.1:g.51182G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298832.14:c.656-234G>A MANE Select ENSP00000298832.9:n.656-234G>A
ENST00000286650.9:c.656-234G>A ENSP00000286650.5:n.656-234G>A
ENST00000298832.13:c.656-234G>A ENSP00000298832.9:n.656-234G>A
ENST00000555422.5:n.125-234G>A
ENST00000556173.5:n.582-234G>A
ENST00000557636.5:c.656-234G>A ENSP00000450713.1:n.656-234G>A
NM_015072.4:c.656-234G>A NP_055887.3:n.656-234G>A
NM_015072.5:c.656-234G>A MANE Select NP_055887.3:n.656-234G>A
Search 100 bp 5'
Search 100 bp 3'