Canonical Allele Identifier: CA8562443
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs560760659

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583201_41583202insT , CM000679.2:g.41583201_41583202insT GRCh38
NC_000017.10:g.39739453_39739454insT , CM000679.1:g.39739453_39739454insT GRCh37
NC_000017.9:g.36992979_36992980insT NCBI36
NG_008624.1:g.8694_8695insA

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+33_1274+34insA MANE Select ENSP00000167586.6:n.1274+33_1274+34insA
ENST00000167586.6:c.1274+33_1274+34insA ENSP00000167586.6:n.1274+33_1274+34insA
ENST00000441550.2:n.221+33_221+34insA
NM_000526.4:c.1274+33_1274+34insA NP_000517.2:n.1274+33_1274+34insA
NM_000526.5:c.1274+33_1274+34insA MANE Select NP_000517.3:n.1274+33_1274+34insA