Canonical Allele Identifier: CA2260085221
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583114C= , CM000679.2:g.41583114C= GRCh38
NC_000017.10:g.39739366C= , CM000679.1:g.39739366C= GRCh37
NC_000017.9:g.36992892C= NCBI36
NG_008624.1:g.8782G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1301G= MANE Select ENSP00000167586.6:p.Gly434=
ENST00000167586.6:c.1301G= ENSP00000167586.6:p.Gly434=
ENST00000441550.2:n.248G=
NM_000526.4:c.1301G= NP_000517.2:p.Gly434=
NM_000526.5:c.1301G= MANE Select NP_000517.3:p.Gly434=
Search 100 bp 5'
Search 100 bp 3'