Canonical Allele Identifier: CA2260086757
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586300A= , CM000679.2:g.41586300A= GRCh38
NC_000017.10:g.39742552A= , CM000679.1:g.39742552A= GRCh37
NC_000017.9:g.36996078A= NCBI36
NG_008624.1:g.5596T=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+10T= MANE Select ENSP00000167586.6:n.525+10T=
ENST00000167586.6:c.525+10T= ENSP00000167586.6:n.525+10T=
NM_000526.4:c.525+10T= NP_000517.2:n.525+10T=
NM_000526.5:c.525+10T= MANE Select NP_000517.3:n.525+10T=
Search 100 bp 5'
Search 100 bp 3'