Canonical Allele Identifier: CA913190741
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 623897
ClinVar RCV Id: RCV000761951
dbSNP Id: rs1567738332
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586795del , CM000679.2:g.41586795del GRCh38
NC_000017.10:g.39743047del , CM000679.1:g.39743047del GRCh37
NC_000017.9:g.36996573del NCBI36
NG_008624.1:g.5101del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.40del MANE Select ENSP00000167586.6:p.Met14Ter
ENST00000167586.6:c.40del ENSP00000167586.6:p.Met14Ter
NM_000526.4:c.40del NP_000517.2:p.Met14Ter
NM_000526.5:c.40del MANE Select NP_000517.3:p.Met14Ter
Search 100 bp 5'
Search 100 bp 3'