Canonical Allele Identifier: CA2260085336
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583300G= , CM000679.2:g.41583300G= GRCh38
NC_000017.10:g.39739552G= , CM000679.1:g.39739552G= GRCh37
NC_000017.9:g.36993078G= NCBI36
NG_008624.1:g.8596C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1209C= MANE Select ENSP00000167586.6:p.Asp403=
ENST00000167586.6:c.1209C= ENSP00000167586.6:p.Asp403=
ENST00000441550.2:n.156C=
ENST00000476662.1:n.659C=
NM_000526.4:c.1209C= NP_000517.2:p.Asp403=
NM_000526.5:c.1209C= MANE Select NP_000517.3:p.Asp403=