Canonical Allele Identifier: CA2147608624
Gene: TTLL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707390T= , CM000676.2:g.75707390T= GRCh38
NC_000014.8:g.76173733T= , CM000676.1:g.76173733T= GRCh37
NC_000014.7:g.75243486T= NCBI36
NG_016974.1:g.51183T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.656-233T= MANE Select ENSP00000298832.9:n.656-233T=
ENST00000286650.9:c.656-233T= ENSP00000286650.5:n.656-233T=
ENST00000298832.13:c.656-233T= ENSP00000298832.9:n.656-233T=
ENST00000555422.5:n.125-233T=
ENST00000556173.5:n.582-233T=
ENST00000557636.5:c.656-233T= ENSP00000450713.1:n.656-233T=
NM_015072.4:c.656-233T= NP_055887.3:n.656-233T=
NM_015072.5:c.656-233T= MANE Select NP_055887.3:n.656-233T=