Canonical Allele Identifier: CA366424172
Gene: TTLL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341158C>G , CM000668.2:g.167341158C>G GRCh38
NC_000006.11:g.167754646C>G , CM000668.1:g.167754646C>G GRCh37
NC_000006.10:g.167674636C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1258C>G MANE Select ENSP00000239587.5:p.Leu420Val
ENST00000649884.1:c.1039C>G ENSP00000497040.1:p.Leu347Val
ENST00000239587.9:c.1258C>G ENSP00000239587.5:p.Leu420Val
ENST00000515138.1:c.1258C>G ENSP00000424130.1:p.Leu420Val
NM_031949.4:c.1258C>G NP_114155.4:p.Leu420Val
XM_006715572.2:c.1039C>G XP_006715635.1:p.Leu347Val
XM_006715572.4:c.1039C>G XP_006715635.1:p.Leu347Val
NM_031949.5:c.1258C>G MANE Select NP_114155.4:p.Leu420Val