Canonical Allele Identifier: CA366425119
Gene: TTLL2 HGNC NCBI

Linked Data

COSMIC: COSM1268867
MyVariant Identifiers: chr6:g.167755087C>A (hg19) chr6:g.167341599C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341599C>A , CM000668.2:g.167341599C>A GRCh38
NC_000006.11:g.167755087C>A , CM000668.1:g.167755087C>A GRCh37
NC_000006.10:g.167675077C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1699C>A MANE Select ENSP00000239587.5:p.Leu567Ile
ENST00000649884.1:c.1480C>A ENSP00000497040.1:p.Leu494Ile
ENST00000239587.9:c.1699C>A ENSP00000239587.5:p.Leu567Ile
ENST00000515138.1:c.1699C>A ENSP00000424130.1:p.Leu567Ile
NM_031949.4:c.1699C>A NP_114155.4:p.Leu567Ile
XM_006715572.2:c.1480C>A XP_006715635.1:p.Leu494Ile
XM_006715572.4:c.1480C>A XP_006715635.1:p.Leu494Ile
NM_031949.5:c.1699C>A MANE Select NP_114155.4:p.Leu567Ile
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