Canonical Allele Identifier: CA216892
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66337
ClinVar RCV Id: RCV000015732 RCV000056703
dbSNP Id: rs57278315
MyVariant Identifiers: chr17:g.39742773_39742774del (hg19) chr17:g.41586521_41586522del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586521_41586522del , CM000679.2:g.41586521_41586522del GRCh38
NC_000017.10:g.39742773_39742774del , CM000679.1:g.39742773_39742774del GRCh37
NC_000017.9:g.36996299_36996300del NCBI36
NG_008624.1:g.5374_5375del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.313_314del MANE Select ENSP00000167586.6:p.Ala105TrpfsTer3
ENST00000167586.6:c.313_314del ENSP00000167586.6:p.Ala105TrpfsTer3
NM_000526.4:c.313_314del NP_000517.2:p.Ala105TrpfsTer3
NM_000526.5:c.313_314del MANE Select NP_000517.3:p.Ala105TrpfsTer3
Search 100 bp 5'
Search 100 bp 3'