Canonical Allele Identifier: CA216956
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66366
ClinVar RCV Id: RCV000056737
dbSNP Id: rs57180772

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586409del , CM000679.2:g.41586409del GRCh38
NC_000017.10:g.39742661del , CM000679.1:g.39742661del GRCh37
NC_000017.9:g.36996187del NCBI36
NG_008624.1:g.5488del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.427del MANE Select ENSP00000167586.6:p.Leu143TrpfsTer3
ENST00000167586.6:c.427del ENSP00000167586.6:p.Leu143TrpfsTer3
NM_000526.4:c.427del NP_000517.2:p.Leu143TrpfsTer3
NM_000526.5:c.427del MANE Select NP_000517.3:p.Leu143TrpfsTer3