Canonical Allele Identifier: CA2260085928
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584413C= , CM000679.2:g.41584413C= GRCh38
NC_000017.10:g.39740665C= , CM000679.1:g.39740665C= GRCh37
NC_000017.9:g.36994191C= NCBI36
NG_008624.1:g.7483G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609G= MANE Select ENSP00000167586.6:p.Lys203=
ENST00000167586.6:c.609G= ENSP00000167586.6:p.Lys203=
ENST00000476662.1:n.59G=
NM_000526.4:c.609G= NP_000517.2:p.Lys203=
NM_000526.5:c.609G= MANE Select NP_000517.3:p.Lys203=