Canonical Allele Identifier: CA2260086050
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584671G= , CM000679.2:g.41584671G= GRCh38
NC_000017.10:g.39740923G= , CM000679.1:g.39740923G= GRCh37
NC_000017.9:g.36994449G= NCBI36
NG_008624.1:g.7225C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-258C= MANE Select ENSP00000167586.6:n.609-258C=
ENST00000167586.6:c.609-258C= ENSP00000167586.6:n.609-258C=
NM_000526.4:c.609-258C= NP_000517.2:n.609-258C=
NM_000526.5:c.609-258C= MANE Select NP_000517.3:n.609-258C=
Search 100 bp 5'
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