Canonical Allele Identifier: CA366425152
Gene: TTLL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341615A>C , CM000668.2:g.167341615A>C GRCh38
NC_000006.11:g.167755103A>C , CM000668.1:g.167755103A>C GRCh37
NC_000006.10:g.167675093A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1715A>C MANE Select ENSP00000239587.5:p.Asn572Thr
ENST00000649884.1:c.1496A>C ENSP00000497040.1:p.Asn499Thr
ENST00000239587.9:c.1715A>C ENSP00000239587.5:p.Asn572Thr
ENST00000515138.1:c.1715A>C ENSP00000424130.1:p.Asn572Thr
NM_031949.4:c.1715A>C NP_114155.4:p.Asn572Thr
XM_006715572.2:c.1496A>C XP_006715635.1:p.Asn499Thr
XM_006715572.4:c.1496A>C XP_006715635.1:p.Asn499Thr
NM_031949.5:c.1715A>C MANE Select NP_114155.4:p.Asn572Thr