Canonical Allele Identifier: CA1680342114
Gene: TTLL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341460A= , CM000668.2:g.167341460A= GRCh38
NC_000006.11:g.167754948A= , CM000668.1:g.167754948A= GRCh37
NC_000006.10:g.167674938A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1560A= MANE Select ENSP00000239587.5:p.Thr520=
ENST00000649884.1:c.1341A= ENSP00000497040.1:p.Thr447=
ENST00000239587.9:c.1560A= ENSP00000239587.5:p.Thr520=
ENST00000515138.1:c.1560A= ENSP00000424130.1:p.Thr520=
NM_031949.4:c.1560A= NP_114155.4:p.Thr520=
XM_006715572.2:c.1341A= XP_006715635.1:p.Thr447=
XM_006715572.4:c.1341A= XP_006715635.1:p.Thr447=
NM_031949.5:c.1560A= MANE Select NP_114155.4:p.Thr520=