Canonical Allele Identifier: CA2260085561
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583766G= , CM000679.2:g.41583766G= GRCh38
NC_000017.10:g.39740018G= , CM000679.1:g.39740018G= GRCh37
NC_000017.9:g.36993544G= NCBI36
NG_008624.1:g.8130C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.921C= MANE Select ENSP00000167586.6:p.Phe307=
ENST00000167586.6:c.921C= ENSP00000167586.6:p.Phe307=
ENST00000476662.1:n.371C=
NM_000526.4:c.921C= NP_000517.2:p.Phe307=
NM_000526.5:c.921C= MANE Select NP_000517.3:p.Phe307=
Search 100 bp 5'
Search 100 bp 3'