Canonical Allele Identifier: CA2260086760
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586307C= , CM000679.2:g.41586307C= GRCh38
NC_000017.10:g.39742559C= , CM000679.1:g.39742559C= GRCh37
NC_000017.9:g.36996085C= NCBI36
NG_008624.1:g.5589G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+3G= MANE Select ENSP00000167586.6:n.525+3G=
ENST00000167586.6:c.525+3G= ENSP00000167586.6:n.525+3G=
NM_000526.4:c.525+3G= NP_000517.2:n.525+3G=
NM_000526.5:c.525+3G= MANE Select NP_000517.3:n.525+3G=
Search 100 bp 5'
Search 100 bp 3'