Canonical Allele Identifier: CA645584609
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583093_41583094delinsTT , CM000679.2:g.41583093_41583094delinsTT GRCh38
NC_000017.10:g.39739345_39739346delinsTT , CM000679.1:g.39739345_39739346delinsTT GRCh37
NC_000017.9:g.36992871_36992872delinsTT NCBI36
NG_008624.1:g.8802_8803delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1321_1321+1delinsAA
ENST00000167586.6:c.1321_1321+1delinsAA
ENST00000441550.2:n.268_269delinsAA
NM_000526.4:c.1321_1321+1delinsAA
NM_000526.5:c.1321_1321+1delinsAA