Canonical Allele Identifier: CA216841
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66311
ClinVar RCV Id: RCV000056674
dbSNP Id: rs58397858
MyVariant Identifiers: chr17:g.39739543del (hg19) chr17:g.41583291del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583291del , CM000679.2:g.41583291del GRCh38
NC_000017.10:g.39739543del , CM000679.1:g.39739543del GRCh37
NC_000017.9:g.36993069del NCBI36
NG_008624.1:g.8605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1218del MANE Select ENSP00000167586.6:p.Arg407GlyfsTer?
ENST00000167586.6:c.1218del ENSP00000167586.6:p.Arg407GlyfsTer?
ENST00000441550.2:n.165del
ENST00000476662.1:n.668del
NM_000526.4:c.1218del NP_000517.2:p.Arg407GlyfsTer?
NM_000526.5:c.1218del MANE Select NP_000517.3:p.Arg407GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'