Canonical Allele Identifier: CA2637836284
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41584400-ACT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584403_41584404del , CM000679.2:g.41584403_41584404del GRCh38
NC_000017.10:g.39740655_39740656del , CM000679.1:g.39740655_39740656del GRCh37
NC_000017.9:g.36994181_36994182del NCBI36
NG_008624.1:g.7494_7495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.620_621del MANE Select ENSP00000167586.6:p.Glu207ValfsTer27
ENST00000167586.6:c.620_621del ENSP00000167586.6:p.Glu207ValfsTer27
ENST00000476662.1:n.70_71del
NM_000526.4:c.620_621del NP_000517.2:p.Glu207ValfsTer27
NM_000526.5:c.620_621del MANE Select NP_000517.3:p.Glu207ValfsTer27
Search 100 bp 5'
Search 100 bp 3'