Canonical Allele Identifier: CA1680342007
Gene: TTLL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341216_167341217delinsCT , CM000668.2:g.167341216_167341217delinsCT GRCh38
NC_000006.11:g.167754704_167754705delinsCT , CM000668.1:g.167754704_167754705delinsCT GRCh37
NC_000006.10:g.167674694_167674695delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1316_1317delinsCT MANE Select ENSP00000239587.5:p.Ala439=
ENST00000649884.1:c.1097_1098delinsCT ENSP00000497040.1:p.Ala366=
ENST00000239587.9:c.1316_1317delinsCT ENSP00000239587.5:p.Ala439=
ENST00000515138.1:c.1316_1317delinsCT ENSP00000424130.1:p.Ala439=
NM_031949.4:c.1316_1317delinsCT NP_114155.4:p.Ala439=
XM_006715572.2:c.1097_1098delinsCT XP_006715635.1:p.Ala366=
XM_006715572.4:c.1097_1098delinsCT XP_006715635.1:p.Ala366=
NM_031949.5:c.1316_1317delinsCT MANE Select NP_114155.4:p.Ala439=
Search 100 bp 5'
Search 100 bp 3'