Canonical Allele Identifier: CA1680342173
Gene: TTLL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341602G= , CM000668.2:g.167341602G= GRCh38
NC_000006.11:g.167755090G= , CM000668.1:g.167755090G= GRCh37
NC_000006.10:g.167675080G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1702G= MANE Select ENSP00000239587.5:p.Gly568=
ENST00000649884.1:c.1483G= ENSP00000497040.1:p.Gly495=
ENST00000239587.9:c.1702G= ENSP00000239587.5:p.Gly568=
ENST00000515138.1:c.1702G= ENSP00000424130.1:p.Gly568=
NM_031949.4:c.1702G= NP_114155.4:p.Gly568=
XM_006715572.2:c.1483G= XP_006715635.1:p.Gly495=
XM_006715572.4:c.1483G= XP_006715635.1:p.Gly495=
NM_031949.5:c.1702G= MANE Select NP_114155.4:p.Gly568=