Canonical Allele Identifier: CA2260085118
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41582976G= , CM000679.2:g.41582976G= GRCh38
NC_000017.10:g.39739228G= , CM000679.1:g.39739228G= GRCh37
NC_000017.9:g.36992754G= NCBI36
NG_008624.1:g.8920C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+118C= MANE Select ENSP00000167586.6:n.1321+118C=
ENST00000167586.6:c.1321+118C= ENSP00000167586.6:n.1321+118C=
ENST00000441550.2:n.386C=
NM_000526.4:c.1321+118C= NP_000517.2:n.1321+118C=
NM_000526.5:c.1321+118C= MANE Select NP_000517.3:n.1321+118C=