Canonical Allele Identifier: CA2260087029
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586771_41586783delinsCCCCGATGCCGCA , CM000679.2:g.41586771_41586783delinsCCCCGATGCCGCA GRCh38
NC_000017.10:g.39743023_39743035delinsCCCCGATGCCGCA , CM000679.1:g.39743023_39743035delinsCCCCGATGCCGCA GRCh37
NC_000017.9:g.36996549_36996561delinsCCCCGATGCCGCA NCBI36
NG_008624.1:g.5113_5125delinsTGCGGCATCGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.52_64delinsTGCGGCATCGGGG MANE Select ENSP00000167586.6:p.Cys18=
ENST00000167586.6:c.52_64delinsTGCGGCATCGGGG ENSP00000167586.6:p.Cys18=
NM_000526.4:c.52_64delinsTGCGGCATCGGGG NP_000517.2:p.Cys18=
NM_000526.5:c.52_64delinsTGCGGCATCGGGG MANE Select NP_000517.3:p.Cys18=
Search 100 bp 5'
Search 100 bp 3'