Canonical Allele Identifier: CA2260086944
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586648A= , CM000679.2:g.41586648A= GRCh38
NC_000017.10:g.39742900A= , CM000679.1:g.39742900A= GRCh37
NC_000017.9:g.36996426A= NCBI36
NG_008624.1:g.5248T=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.187T= MANE Select ENSP00000167586.6:p.Cys63=
ENST00000167586.6:c.187T= ENSP00000167586.6:p.Cys63=
NM_000526.4:c.187T= NP_000517.2:p.Tyr63=
NM_000526.5:c.187T= MANE Select NP_000517.3:p.Cys63=