Canonical Allele Identifier: CA2695225875
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583254del , CM000679.2:g.41583254del GRCh38
NC_000017.10:g.39739506del , CM000679.1:g.39739506del GRCh37
NC_000017.9:g.36993032del NCBI36
NG_008624.1:g.8642del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1255del MANE Select ENSP00000167586.6:p.Leu419TrpfsTer23
ENST00000167586.6:c.1255del ENSP00000167586.6:p.Leu419TrpfsTer23
ENST00000441550.2:n.202del
ENST00000476662.1:n.705del
NM_000526.4:c.1255del NP_000517.2:p.Leu419TrpfsTer23
NM_000526.5:c.1255del MANE Select NP_000517.3:p.Leu419TrpfsTer23
Search 100 bp 5'
Search 100 bp 3'