Canonical Allele Identifier: CA366423981
Gene: TTLL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341071C>T , CM000668.2:g.167341071C>T GRCh38
NC_000006.11:g.167754559C>T , CM000668.1:g.167754559C>T GRCh37
NC_000006.10:g.167674549C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1171C>T MANE Select ENSP00000239587.5:p.Pro391Ser
ENST00000649884.1:c.952C>T ENSP00000497040.1:p.Pro318Ser
ENST00000239587.9:c.1171C>T ENSP00000239587.5:p.Pro391Ser
ENST00000515138.1:c.1171C>T ENSP00000424130.1:p.Pro391Ser
NM_031949.4:c.1171C>T NP_114155.4:p.Pro391Ser
XM_006715572.2:c.952C>T XP_006715635.1:p.Pro318Ser
XM_006715572.4:c.952C>T XP_006715635.1:p.Pro318Ser
NM_031949.5:c.1171C>T MANE Select NP_114155.4:p.Pro391Ser