Canonical Allele Identifier: CA366424080
Gene: TTLL2 HGNC NCBI

Linked Data

gnomAD v4: 6-167341117-A-G
MyVariant Identifiers: chr6:g.167754605A>G (hg19) chr6:g.167341117A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341117A>G , CM000668.2:g.167341117A>G GRCh38
NC_000006.11:g.167754605A>G , CM000668.1:g.167754605A>G GRCh37
NC_000006.10:g.167674595A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1217A>G MANE Select ENSP00000239587.5:p.Lys406Arg
ENST00000649884.1:c.998A>G ENSP00000497040.1:p.Lys333Arg
ENST00000239587.9:c.1217A>G ENSP00000239587.5:p.Lys406Arg
ENST00000515138.1:c.1217A>G ENSP00000424130.1:p.Lys406Arg
NM_031949.4:c.1217A>G NP_114155.4:p.Lys406Arg
XM_006715572.2:c.998A>G XP_006715635.1:p.Lys333Arg
XM_006715572.4:c.998A>G XP_006715635.1:p.Lys333Arg
NM_031949.5:c.1217A>G MANE Select NP_114155.4:p.Lys406Arg
Search 100 bp 5'
Search 100 bp 3'