Canonical Allele Identifier: CA216994
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66385
dbSNP Id: rs60231560

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586743del , CM000679.2:g.41586743del GRCh38
NC_000017.10:g.39742995del , CM000679.1:g.39742995del GRCh37
NC_000017.9:g.36996521del NCBI36
NG_008624.1:g.5153del

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.92del MANE Select ENSP00000167586.6:p.Ile31ThrfsTer?
ENST00000167586.6:c.92del ENSP00000167586.6:p.Ile31ThrfsTer?
NM_000526.4:c.92del NP_000517.2:p.Ile31ThrfsTer?
NM_000526.5:c.92del MANE Select NP_000517.3:p.Ile31ThrfsTer?