Canonical Allele Identifier: CA1680342181
Gene: TTLL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341630_167341633delinsAAAG , CM000668.2:g.167341630_167341633delinsAAAG GRCh38
NC_000006.11:g.167755118_167755121delinsAAAG , CM000668.1:g.167755118_167755121delinsAAAG GRCh37
NC_000006.10:g.167675108_167675111delinsAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1730_1733delinsAAAG MANE Select ENSP00000239587.5:p.Lys577=
ENST00000649884.1:c.1511_1514delinsAAAG ENSP00000497040.1:p.Lys504=
ENST00000239587.9:c.1730_1733delinsAAAG ENSP00000239587.5:p.Lys577=
ENST00000515138.1:c.1730_1733delinsAAAG ENSP00000424130.1:p.Lys577=
NM_031949.4:c.1730_1733delinsAAAG NP_114155.4:p.Lys577=
XM_006715572.2:c.1511_1514delinsAAAG XP_006715635.1:p.Lys504=
XM_006715572.4:c.1511_1514delinsAAAG XP_006715635.1:p.Lys504=
NM_031949.5:c.1730_1733delinsAAAG MANE Select NP_114155.4:p.Lys577=
Search 100 bp 5'
Search 100 bp 3'