Canonical Allele Identifier: CA2773968270
Gene: TTLL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341107dup , CM000668.2:g.167341107dup GRCh38
NC_000006.11:g.167754595dup , CM000668.1:g.167754595dup GRCh37
NC_000006.10:g.167674585dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1207dup MANE Select ENSP00000239587.5:p.Val403GlyfsTer8
ENST00000649884.1:c.988dup ENSP00000497040.1:p.Val330GlyfsTer8
ENST00000239587.9:c.1207dup ENSP00000239587.5:p.Val403GlyfsTer8
ENST00000515138.1:c.1207dup ENSP00000424130.1:p.Val403GlyfsTer8
NM_031949.4:c.1207dup NP_114155.4:p.Val403GlyfsTer8
XM_006715572.2:c.988dup XP_006715635.1:p.Val330GlyfsTer8
XM_006715572.4:c.988dup XP_006715635.1:p.Val330GlyfsTer8
NM_031949.5:c.1207dup MANE Select NP_114155.4:p.Val403GlyfsTer8
Search 100 bp 5'
Search 100 bp 3'