Canonical Allele Identifier: CA366424159
Gene: TTLL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341152A>G , CM000668.2:g.167341152A>G GRCh38
NC_000006.11:g.167754640A>G , CM000668.1:g.167754640A>G GRCh37
NC_000006.10:g.167674630A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1252A>G MANE Select ENSP00000239587.5:p.Asn418Asp
ENST00000649884.1:c.1033A>G ENSP00000497040.1:p.Asn345Asp
ENST00000239587.9:c.1252A>G ENSP00000239587.5:p.Asn418Asp
ENST00000515138.1:c.1252A>G ENSP00000424130.1:p.Asn418Asp
NM_031949.4:c.1252A>G NP_114155.4:p.Asn418Asp
XM_006715572.2:c.1033A>G XP_006715635.1:p.Asn345Asp
XM_006715572.4:c.1033A>G XP_006715635.1:p.Asn345Asp
NM_031949.5:c.1252A>G MANE Select NP_114155.4:p.Asn418Asp