Canonical Allele Identifier: CA2260086941
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586645_41586647delinsCGC , CM000679.2:g.41586645_41586647delinsCGC GRCh38
NC_000017.10:g.39742897_39742899delinsCGC , CM000679.1:g.39742897_39742899delinsCGC GRCh37
NC_000017.9:g.36996423_36996425delinsCGC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.188_190delinsGCG MANE Select ENSP00000167586.6:p.Cys63=
ENST00000167586.6:c.188_190delinsGCG ENSP00000167586.6:p.Cys63=
NM_000526.5:c.188_190delinsGCG MANE Select NP_000517.3:p.Cys63=