Canonical Allele Identifier: CA2260086942
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586646G= , CM000679.2:g.41586646G= GRCh38
NC_000017.10:g.39742898G= , CM000679.1:g.39742898G= GRCh37
NC_000017.9:g.36996424G= NCBI36
NG_008624.1:g.5250C=

Transcript Alleles

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