Canonical Allele Identifier: CA919841706
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1555572089

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586646_41586647delinsA , CM000679.2:g.41586646_41586647delinsA GRCh38
NC_000017.10:g.39742898_39742899delinsA , CM000679.1:g.39742898_39742899delinsA GRCh37
NC_000017.9:g.36996424_36996425delinsA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.188_189delinsT MANE Select ENSP00000167586.6:p.Cys63LeufsTer?
ENST00000167586.6:c.188_189delinsT ENSP00000167586.6:p.Cys63LeufsTer?
NM_000526.5:c.188_189delinsT MANE Select NP_000517.3:p.Cys63LeufsTer?