Canonical Allele Identifier: CA919841707
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1555572096

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586647del , CM000679.2:g.41586647del GRCh38
NC_000017.10:g.39742899del , CM000679.1:g.39742899del GRCh37
NC_000017.9:g.36996425del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.188del MANE Select ENSP00000167586.6:p.Cys63SerfsTer?
ENST00000167586.6:c.188del ENSP00000167586.6:p.Cys63SerfsTer?
NM_000526.5:c.188del MANE Select NP_000517.3:p.Cys63SerfsTer?