Canonical Allele Identifier: CA2576267747
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583132del , CM000679.2:g.41583132del GRCh38
NC_000017.10:g.39739384del , CM000679.1:g.39739384del GRCh37
NC_000017.9:g.36992910del NCBI36
NG_008624.1:g.8765del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1284del MANE Select ENSP00000167586.6:p.Ser429ProfsTer13
ENST00000167586.6:c.1284del ENSP00000167586.6:p.Ser429ProfsTer13
ENST00000441550.2:n.231del
NM_000526.4:c.1284del NP_000517.2:p.Ser429ProfsTer13
NM_000526.5:c.1284del MANE Select NP_000517.3:p.Ser429ProfsTer13