Canonical Allele Identifier: CA2147608612
Gene: TTLL5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707359G= , CM000676.2:g.75707359G= GRCh38
NC_000014.8:g.76173702G= , CM000676.1:g.76173702G= GRCh37
NC_000014.7:g.75243455G= NCBI36
NG_016974.1:g.51152G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.656-264G= MANE Select ENSP00000298832.9:n.656-264G=
ENST00000286650.9:c.656-264G= ENSP00000286650.5:n.656-264G=
ENST00000298832.13:c.656-264G= ENSP00000298832.9:n.656-264G=
ENST00000555422.5:n.125-264G=
ENST00000556173.5:n.582-264G=
ENST00000557636.5:c.656-264G= ENSP00000450713.1:n.656-264G=
NM_015072.4:c.656-264G= NP_055887.3:n.656-264G=
NM_015072.5:c.656-264G= MANE Select NP_055887.3:n.656-264G=
Search 100 bp 5'
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