Canonical Allele Identifier: CA2260085313
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583267G= , CM000679.2:g.41583267G= GRCh38
NC_000017.10:g.39739519G= , CM000679.1:g.39739519G= GRCh37
NC_000017.9:g.36993045G= NCBI36
NG_008624.1:g.8629C=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1242C= MANE Select ENSP00000167586.6:p.Thr414=
ENST00000167586.6:c.1242C= ENSP00000167586.6:p.Thr414=
ENST00000441550.2:n.189C=
ENST00000476662.1:n.692C=
NM_000526.4:c.1242C= NP_000517.2:p.Thr414=
NM_000526.5:c.1242C= MANE Select NP_000517.3:p.Thr414=