Canonical Allele Identifier: CA772041234
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1431871082

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586763del , CM000679.2:g.41586763del GRCh38
NC_000017.10:g.39743015del , CM000679.1:g.39743015del GRCh37
NC_000017.9:g.36996541del NCBI36
NG_008624.1:g.5133del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.72del MANE Select ENSP00000167586.6:p.Ile24MetfsTer?
ENST00000167586.6:c.72del ENSP00000167586.6:p.Ile24MetfsTer?
NM_000526.4:c.72del NP_000517.2:p.Ile24MetfsTer?
NM_000526.5:c.72del MANE Select NP_000517.3:p.Ile24MetfsTer?