Canonical Allele Identifier: CA8562792
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs772964320

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586646_41586647del , CM000679.2:g.41586646_41586647del GRCh38
NC_000017.10:g.39742898_39742899del , CM000679.1:g.39742898_39742899del GRCh37
NC_000017.9:g.36996424_36996425del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.189_190del MANE Select ENSP00000167586.6:p.Cys63TrpfsTer19
ENST00000167586.6:c.189_190del ENSP00000167586.6:p.Cys63TrpfsTer19
NM_000526.5:c.189_190del MANE Select NP_000517.3:p.Cys63TrpfsTer19