Canonical Allele Identifier: CA366425139
Gene: TTLL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341609C>T , CM000668.2:g.167341609C>T GRCh38
NC_000006.11:g.167755097C>T , CM000668.1:g.167755097C>T GRCh37
NC_000006.10:g.167675087C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1709C>T MANE Select ENSP00000239587.5:p.Ser570Phe
ENST00000649884.1:c.1490C>T ENSP00000497040.1:p.Ser497Phe
ENST00000239587.9:c.1709C>T ENSP00000239587.5:p.Ser570Phe
ENST00000515138.1:c.1709C>T ENSP00000424130.1:p.Ser570Phe
NM_031949.4:c.1709C>T NP_114155.4:p.Ser570Phe
XM_006715572.2:c.1490C>T XP_006715635.1:p.Ser497Phe
XM_006715572.4:c.1490C>T XP_006715635.1:p.Ser497Phe
NM_031949.5:c.1709C>T MANE Select NP_114155.4:p.Ser570Phe