Canonical Allele Identifier: CA453304992
Gene: TTLL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.167754564C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341076C>A , CM000668.2:g.167341076C>A GRCh38
NC_000006.11:g.167754564C>A , CM000668.1:g.167754564C>A GRCh37
NC_000006.10:g.167674554C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1176C>A MANE Select ENSP00000239587.5:p.Ala392=
ENST00000649884.1:c.957C>A ENSP00000497040.1:p.Ala319=
ENST00000239587.9:c.1176C>A ENSP00000239587.5:p.Ala392=
ENST00000515138.1:c.1176C>A ENSP00000424130.1:p.Ala392=
NM_031949.4:c.1176C>A NP_114155.4:p.Ala392=
XM_006715572.2:c.957C>A XP_006715635.1:p.Ala319=
XM_006715572.4:c.957C>A XP_006715635.1:p.Ala319=
NM_031949.5:c.1176C>A MANE Select NP_114155.4:p.Ala392=
Search 100 bp 5'
Search 100 bp 3'