Canonical Allele Identifier: CA366424008
Gene: TTLL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341086G>A , CM000668.2:g.167341086G>A GRCh38
NC_000006.11:g.167754574G>A , CM000668.1:g.167754574G>A GRCh37
NC_000006.10:g.167674564G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1186G>A MANE Select ENSP00000239587.5:p.Asp396Asn
ENST00000649884.1:c.967G>A ENSP00000497040.1:p.Asp323Asn
ENST00000239587.9:c.1186G>A ENSP00000239587.5:p.Asp396Asn
ENST00000515138.1:c.1186G>A ENSP00000424130.1:p.Asp396Asn
NM_031949.4:c.1186G>A NP_114155.4:p.Asp396Asn
XM_006715572.2:c.967G>A XP_006715635.1:p.Asp323Asn
XM_006715572.4:c.967G>A XP_006715635.1:p.Asp323Asn
NM_031949.5:c.1186G>A MANE Select NP_114155.4:p.Asp396Asn