Canonical Allele Identifier: CA1680341978
Gene: TTLL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341166_167341168delinsTGA , CM000668.2:g.167341166_167341168delinsTGA GRCh38
NC_000006.11:g.167754654_167754656delinsTGA , CM000668.1:g.167754654_167754656delinsTGA GRCh37
NC_000006.10:g.167674644_167674646delinsTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1266_1268delinsTGA MANE Select ENSP00000239587.5:p.Asn422=
ENST00000649884.1:c.1047_1049delinsTGA ENSP00000497040.1:p.Asn349=
ENST00000239587.9:c.1266_1268delinsTGA ENSP00000239587.5:p.Asn422=
ENST00000515138.1:c.1266_1268delinsTGA ENSP00000424130.1:p.Asn422=
NM_031949.4:c.1266_1268delinsTGA NP_114155.4:p.Asn422=
XM_006715572.2:c.1047_1049delinsTGA XP_006715635.1:p.Asn349=
XM_006715572.4:c.1047_1049delinsTGA XP_006715635.1:p.Asn349=
NM_031949.5:c.1266_1268delinsTGA MANE Select NP_114155.4:p.Asn422=