Canonical Allele Identifier: CA2260085348
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583314_41583315delinsTG , CM000679.2:g.41583314_41583315delinsTG GRCh38
NC_000017.10:g.39739566_39739567delinsTG , CM000679.1:g.39739566_39739567delinsTG GRCh37
NC_000017.9:g.36993092_36993093delinsTG NCBI36
NG_008624.1:g.8581_8582delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1194_1195delinsCA MANE Select ENSP00000167586.6:p.Tyr398=
ENST00000167586.6:c.1194_1195delinsCA ENSP00000167586.6:p.Tyr398=
ENST00000441550.2:n.141_142delinsCA
ENST00000476662.1:n.644_645delinsCA
NM_000526.4:c.1194_1195delinsCA NP_000517.2:p.Tyr398=
NM_000526.5:c.1194_1195delinsCA MANE Select NP_000517.3:p.Tyr398=
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