Canonical Allele Identifier: CA645551846
Gene: TTLL2 HGNC NCBI

Linked Data

COSMIC: COSM1442233
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341638_167341640del , CM000668.2:g.167341638_167341640del GRCh38
NC_000006.11:g.167755126_167755128del , CM000668.1:g.167755126_167755128del GRCh37
NC_000006.10:g.167675116_167675118del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1738_1740del MANE Select ENSP00000239587.5:p.Ile580del
ENST00000649884.1:c.1519_1521del ENSP00000497040.1:p.Ile507del
ENST00000239587.9:c.1738_1740del ENSP00000239587.5:p.Ile580del
ENST00000515138.1:c.1738_1740del ENSP00000424130.1:p.Ile580del
NM_031949.4:c.1738_1740del NP_114155.4:p.Ile580del
XM_006715572.2:c.1519_1521del XP_006715635.1:p.Ile507del
XM_006715572.4:c.1519_1521del XP_006715635.1:p.Ile507del
NM_031949.5:c.1738_1740del MANE Select NP_114155.4:p.Ile580del
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