Canonical Allele Identifier: CA8562834
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs776794978
ExAC: 17:39743026 C / CGAT
gnomAD v4: 17-41586774-C-CGAT
MyVariant Identifiers: chr17:g.39743026_39743027insGAT (hg19) chr17:g.41586774_41586775insGAT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586776_41586778dup , CM000679.2:g.41586776_41586778dup GRCh38
NC_000017.10:g.39743028_39743030dup , CM000679.1:g.39743028_39743030dup GRCh37
NC_000017.9:g.36996554_36996556dup NCBI36
NG_008624.1:g.5119_5121dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.58_60dup MANE Select ENSP00000167586.6:p.Ile20_Gly21insIle
ENST00000167586.6:c.58_60dup ENSP00000167586.6:p.Ile20_Gly21insIle
NM_000526.4:c.58_60dup NP_000517.2:p.Ile20_Gly21insIle
NM_000526.5:c.58_60dup MANE Select NP_000517.3:p.Ile20_Gly21insIle
Search 100 bp 5'
Search 100 bp 3'