Canonical Allele Identifier: CA2637837565
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586648_41586649insTG , CM000679.2:g.41586648_41586649insTG GRCh38
NC_000017.10:g.39742900_39742901insTG , CM000679.1:g.39742900_39742901insTG GRCh37
NC_000017.9:g.36996426_36996427insTG NCBI36
NG_008624.1:g.5247_5248insCA

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.186_187insCA MANE Select ENSP00000167586.6:p.Cys63HisfsTer?
ENST00000167586.6:c.186_187insCA ENSP00000167586.6:p.Cys63HisfsTer?
NM_000526.4:c.186_187insCA NP_000517.2:p.Tyr63HisfsTer?
NM_000526.5:c.186_187insCA MANE Select NP_000517.3:p.Cys63HisfsTer?