Canonical Allele Identifier: CA366425244
Gene: TTLL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.167755141A>T (hg19) chr6:g.167341653A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341653A>T , CM000668.2:g.167341653A>T GRCh38
NC_000006.11:g.167755141A>T , CM000668.1:g.167755141A>T GRCh37
NC_000006.10:g.167675131A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1753A>T MANE Select ENSP00000239587.5:p.Lys585Ter
ENST00000649884.1:c.1534A>T ENSP00000497040.1:p.Lys512Ter
ENST00000239587.9:c.1753A>T ENSP00000239587.5:p.Lys585Ter
ENST00000515138.1:c.1753A>T ENSP00000424130.1:p.Lys585Ter
NM_031949.4:c.1753A>T NP_114155.4:p.Lys585Ter
XM_006715572.2:c.1534A>T XP_006715635.1:p.Lys512Ter
XM_006715572.4:c.1534A>T XP_006715635.1:p.Lys512Ter
NM_031949.5:c.1753A>T MANE Select NP_114155.4:p.Lys585Ter
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