Canonical Allele Identifier: CA1680341941
Gene: TTLL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341087_167341088delinsAT , CM000668.2:g.167341087_167341088delinsAT GRCh38
NC_000006.11:g.167754575_167754576delinsAT , CM000668.1:g.167754575_167754576delinsAT GRCh37
NC_000006.10:g.167674565_167674566delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1187_1188delinsAT MANE Select ENSP00000239587.5:p.Asp396=
ENST00000649884.1:c.968_969delinsAT ENSP00000497040.1:p.Asp323=
ENST00000239587.9:c.1187_1188delinsAT ENSP00000239587.5:p.Asp396=
ENST00000515138.1:c.1187_1188delinsAT ENSP00000424130.1:p.Asp396=
NM_031949.4:c.1187_1188delinsAT NP_114155.4:p.Asp396=
XM_006715572.2:c.968_969delinsAT XP_006715635.1:p.Asp323=
XM_006715572.4:c.968_969delinsAT XP_006715635.1:p.Asp323=
NM_031949.5:c.1187_1188delinsAT MANE Select NP_114155.4:p.Asp396=
Search 100 bp 5'
Search 100 bp 3'