Canonical Allele Identifier: CA2260086018
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584607G= , CM000679.2:g.41584607G= GRCh38
NC_000017.10:g.39740859G= , CM000679.1:g.39740859G= GRCh37
NC_000017.9:g.36994385G= NCBI36
NG_008624.1:g.7289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-194C= MANE Select ENSP00000167586.6:n.609-194C=
ENST00000167586.6:c.609-194C= ENSP00000167586.6:n.609-194C=
NM_000526.4:c.609-194C= NP_000517.2:n.609-194C=
NM_000526.5:c.609-194C= MANE Select NP_000517.3:n.609-194C=
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