Canonical Allele Identifier: CA2695225889
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586806del , CM000679.2:g.41586806del GRCh38
NC_000017.10:g.39743058del , CM000679.1:g.39743058del GRCh37
NC_000017.9:g.36996584del NCBI36
NG_008624.1:g.5091del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.30del MANE Select ENSP00000167586.6:p.Ser11ProfsTer4
ENST00000167586.6:c.30del ENSP00000167586.6:p.Ser11ProfsTer4
NM_000526.4:c.30del NP_000517.2:p.Ser11ProfsTer4
NM_000526.5:c.30del MANE Select NP_000517.3:p.Ser11ProfsTer4
Search 100 bp 5'
Search 100 bp 3'