Canonical Allele Identifier: CA2260085270
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583199_41583200delinsTG , CM000679.2:g.41583199_41583200delinsTG GRCh38
NC_000017.10:g.39739451_39739452delinsTG , CM000679.1:g.39739451_39739452delinsTG GRCh37
NC_000017.9:g.36992977_36992978delinsTG NCBI36
NG_008624.1:g.8696_8697delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+35_1274+36delinsCA MANE Select ENSP00000167586.6:n.1274+35_1274+36delins...
ENST00000167586.6:c.1274+35_1274+36delinsCA ENSP00000167586.6:n.1274+35_1274+36delins...
ENST00000441550.2:n.221+35_221+36delinsCA
NM_000526.4:c.1274+35_1274+36delinsCA NP_000517.2:n.1274+35_1274+36delinsCA
NM_000526.5:c.1274+35_1274+36delinsCA MANE Select NP_000517.3:n.1274+35_1274+36delinsCA