Canonical Allele Identifier: CA2260085962
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584469T= , CM000679.2:g.41584469T= GRCh38
NC_000017.10:g.39740721T= , CM000679.1:g.39740721T= GRCh37
NC_000017.9:g.36994247T= NCBI36
NG_008624.1:g.7427A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-56A= MANE Select ENSP00000167586.6:n.609-56A=
ENST00000167586.6:c.609-56A= ENSP00000167586.6:n.609-56A=
ENST00000476662.1:n.3A=
NM_000526.4:c.609-56A= NP_000517.2:n.609-56A=
NM_000526.5:c.609-56A= MANE Select NP_000517.3:n.609-56A=