Canonical Allele Identifier: CA2260085128
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41582997A= , CM000679.2:g.41582997A= GRCh38
NC_000017.10:g.39739249A= , CM000679.1:g.39739249A= GRCh37
NC_000017.9:g.36992775A= NCBI36
NG_008624.1:g.8899T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+97T= MANE Select ENSP00000167586.6:n.1321+97T=
ENST00000167586.6:c.1321+97T= ENSP00000167586.6:n.1321+97T=
ENST00000441550.2:n.365T=
NM_000526.4:c.1321+97T= NP_000517.2:n.1321+97T=
NM_000526.5:c.1321+97T= MANE Select NP_000517.3:n.1321+97T=