Canonical Allele Identifier: CA2260086938
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586644_41586646delinsCCG , CM000679.2:g.41586644_41586646delinsCCG GRCh38
NC_000017.10:g.39742896_39742898delinsCCG , CM000679.1:g.39742896_39742898delinsCCG GRCh37
NC_000017.9:g.36996422_36996424delinsCCG NCBI36
NG_008624.1:g.5250_5252delinsCGG

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.189_191delinsCGG MANE Select ENSP00000167586.6:p.Cys63=
ENST00000167586.6:c.189_191delinsCGG ENSP00000167586.6:p.Cys63=
NM_000526.4:c.189_191delinsCGG NP_000517.2:p.Tyr63=
NM_000526.5:c.189_191delinsCGG MANE Select NP_000517.3:p.Cys63=