Canonical Allele Identifier: CA964833890
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs1886730023

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707368A>G , CM000676.2:g.75707368A>G GRCh38
NC_000014.8:g.76173711A>G , CM000676.1:g.76173711A>G GRCh37
NC_000014.7:g.75243464A>G NCBI36
NG_016974.1:g.51161A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298832.14:c.656-255A>G MANE Select ENSP00000298832.9:n.656-255A>G
ENST00000286650.9:c.656-255A>G ENSP00000286650.5:n.656-255A>G
ENST00000298832.13:c.656-255A>G ENSP00000298832.9:n.656-255A>G
ENST00000555422.5:n.125-255A>G
ENST00000556173.5:n.582-255A>G
ENST00000557636.5:c.656-255A>G ENSP00000450713.1:n.656-255A>G
NM_015072.4:c.656-255A>G NP_055887.3:n.656-255A>G
NM_015072.5:c.656-255A>G MANE Select NP_055887.3:n.656-255A>G