Canonical Allele Identifier: CA2147608603
Gene: TTLL5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707340A= , CM000676.2:g.75707340A= GRCh38
NC_000014.8:g.76173683A= , CM000676.1:g.76173683A= GRCh37
NC_000014.7:g.75243436A= NCBI36
NG_016974.1:g.51133A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.655+253A= MANE Select ENSP00000298832.9:n.655+253A=
ENST00000286650.9:c.655+253A= ENSP00000286650.5:n.655+253A=
ENST00000298832.13:c.655+253A= ENSP00000298832.9:n.655+253A=
ENST00000555422.5:n.124+253A=
ENST00000556173.5:n.581+253A=
ENST00000557636.5:c.655+253A= ENSP00000450713.1:n.655+253A=
NM_015072.4:c.655+253A= NP_055887.3:n.655+253A=
NM_015072.5:c.655+253A= MANE Select NP_055887.3:n.655+253A=
Search 100 bp 5'
Search 100 bp 3'