Canonical Allele Identifier: CA1680342146
Gene: TTLL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341535T= , CM000668.2:g.167341535T= GRCh38
NC_000006.11:g.167755023T= , CM000668.1:g.167755023T= GRCh37
NC_000006.10:g.167675013T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1635T= MANE Select ENSP00000239587.5:p.Arg545=
ENST00000649884.1:c.1416T= ENSP00000497040.1:p.Arg472=
ENST00000239587.9:c.1635T= ENSP00000239587.5:p.Arg545=
ENST00000515138.1:c.1635T= ENSP00000424130.1:p.Arg545=
NM_031949.4:c.1635T= NP_114155.4:p.Arg545=
XM_006715572.2:c.1416T= XP_006715635.1:p.Arg472=
XM_006715572.4:c.1416T= XP_006715635.1:p.Arg472=
NM_031949.5:c.1635T= MANE Select NP_114155.4:p.Arg545=