Canonical Allele Identifier: CA1680342155
Gene: TTLL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341558_167341559delinsCA , CM000668.2:g.167341558_167341559delinsCA GRCh38
NC_000006.11:g.167755046_167755047delinsCA , CM000668.1:g.167755046_167755047delinsCA GRCh37
NC_000006.10:g.167675036_167675037delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1658_1659delinsCA MANE Select ENSP00000239587.5:p.Ala553=
ENST00000649884.1:c.1439_1440delinsCA ENSP00000497040.1:p.Ala480=
ENST00000239587.9:c.1658_1659delinsCA ENSP00000239587.5:p.Ala553=
ENST00000515138.1:c.1658_1659delinsCA ENSP00000424130.1:p.Ala553=
NM_031949.4:c.1658_1659delinsCA NP_114155.4:p.Ala553=
XM_006715572.2:c.1439_1440delinsCA XP_006715635.1:p.Ala480=
XM_006715572.4:c.1439_1440delinsCA XP_006715635.1:p.Ala480=
NM_031949.5:c.1658_1659delinsCA MANE Select NP_114155.4:p.Ala553=