Canonical Allele Identifier: CA2260086016
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584603A= , CM000679.2:g.41584603A= GRCh38
NC_000017.10:g.39740855A= , CM000679.1:g.39740855A= GRCh37
NC_000017.9:g.36994381A= NCBI36
NG_008624.1:g.7293T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-190T= MANE Select ENSP00000167586.6:n.609-190T=
ENST00000167586.6:c.609-190T= ENSP00000167586.6:n.609-190T=
NM_000526.4:c.609-190T= NP_000517.2:n.609-190T=
NM_000526.5:c.609-190T= MANE Select NP_000517.3:n.609-190T=
Search 100 bp 5'
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