Canonical Allele Identifier: CA1680342151
Gene: TTLL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341555_167341558delinsAAGC , CM000668.2:g.167341555_167341558delinsAAGC GRCh38
NC_000006.11:g.167755043_167755046delinsAAGC , CM000668.1:g.167755043_167755046delinsAAGC GRCh37
NC_000006.10:g.167675033_167675036delinsAAGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1655_1658delinsAAGC MANE Select ENSP00000239587.5:p.Gln552=
ENST00000649884.1:c.1436_1439delinsAAGC ENSP00000497040.1:p.Gln479=
ENST00000239587.9:c.1655_1658delinsAAGC ENSP00000239587.5:p.Gln552=
ENST00000515138.1:c.1655_1658delinsAAGC ENSP00000424130.1:p.Gln552=
NM_031949.4:c.1655_1658delinsAAGC NP_114155.4:p.Gln552=
XM_006715572.2:c.1436_1439delinsAAGC XP_006715635.1:p.Gln479=
XM_006715572.4:c.1436_1439delinsAAGC XP_006715635.1:p.Gln479=
NM_031949.5:c.1655_1658delinsAAGC MANE Select NP_114155.4:p.Gln552=
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