Canonical Allele Identifier: CA2260085929
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584414C= , CM000679.2:g.41584414C= GRCh38
NC_000017.10:g.39740666C= , CM000679.1:g.39740666C= GRCh37
NC_000017.9:g.36994192C= NCBI36
NG_008624.1:g.7482G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-1G= MANE Select ENSP00000167586.6:n.609-1G=
ENST00000167586.6:c.609-1G= ENSP00000167586.6:n.609-1G=
ENST00000476662.1:n.58G=
NM_000526.4:c.609-1G= NP_000517.2:n.609-1G=
NM_000526.5:c.609-1G= MANE Select NP_000517.3:n.609-1G=