Canonical Allele Identifier: CA1680342164
Gene: TTLL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341579T= , CM000668.2:g.167341579T= GRCh38
NC_000006.11:g.167755067T= , CM000668.1:g.167755067T= GRCh37
NC_000006.10:g.167675057T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1679T= MANE Select ENSP00000239587.5:p.Phe560=
ENST00000649884.1:c.1460T= ENSP00000497040.1:p.Phe487=
ENST00000239587.9:c.1679T= ENSP00000239587.5:p.Phe560=
ENST00000515138.1:c.1679T= ENSP00000424130.1:p.Phe560=
NM_031949.4:c.1679T= NP_114155.4:p.Phe560=
XM_006715572.2:c.1460T= XP_006715635.1:p.Phe487=
XM_006715572.4:c.1460T= XP_006715635.1:p.Phe487=
NM_031949.5:c.1679T= MANE Select NP_114155.4:p.Phe560=