Canonical Allele Identifier: CA4097510
Gene: TTLL2 HGNC NCBI

Linked Data

dbSNP Id: rs765596268

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341214_167341215insT , CM000668.2:g.167341214_167341215insT GRCh38
NC_000006.11:g.167754702_167754703insT , CM000668.1:g.167754702_167754703insT GRCh37
NC_000006.10:g.167674692_167674693insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1314_1315insT MANE Select ENSP00000239587.5:p.Ala439CysfsTer5
ENST00000649884.1:c.1095_1096insT ENSP00000497040.1:p.Ala366CysfsTer5
ENST00000239587.9:c.1314_1315insT ENSP00000239587.5:p.Ala439CysfsTer5
ENST00000515138.1:c.1314_1315insT ENSP00000424130.1:p.Ala439CysfsTer5
NM_031949.4:c.1314_1315insT NP_114155.4:p.Ala439CysfsTer5
XM_006715572.2:c.1095_1096insT XP_006715635.1:p.Ala366CysfsTer5
XM_006715572.4:c.1095_1096insT XP_006715635.1:p.Ala366CysfsTer5
NM_031949.5:c.1314_1315insT MANE Select NP_114155.4:p.Ala439CysfsTer5