Canonical Allele Identifier: CA453091267
Gene: TTLL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.167755089C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341601C>A , CM000668.2:g.167341601C>A GRCh38
NC_000006.11:g.167755089C>A , CM000668.1:g.167755089C>A GRCh37
NC_000006.10:g.167675079C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1701C>A MANE Select ENSP00000239587.5:p.Leu567=
ENST00000649884.1:c.1482C>A ENSP00000497040.1:p.Leu494=
ENST00000239587.9:c.1701C>A ENSP00000239587.5:p.Leu567=
ENST00000515138.1:c.1701C>A ENSP00000424130.1:p.Leu567=
NM_031949.4:c.1701C>A NP_114155.4:p.Leu567=
XM_006715572.2:c.1482C>A XP_006715635.1:p.Leu494=
XM_006715572.4:c.1482C>A XP_006715635.1:p.Leu494=
NM_031949.5:c.1701C>A MANE Select NP_114155.4:p.Leu567=
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