Canonical Allele Identifier: CA2260085345
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583312C= , CM000679.2:g.41583312C= GRCh38
NC_000017.10:g.39739564C= , CM000679.1:g.39739564C= GRCh37
NC_000017.9:g.36993090C= NCBI36
NG_008624.1:g.8584G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1197G= MANE Select ENSP00000167586.6:p.Lys399=
ENST00000167586.6:c.1197G= ENSP00000167586.6:p.Lys399=
ENST00000441550.2:n.144G=
ENST00000476662.1:n.647G=
NM_000526.4:c.1197G= NP_000517.2:p.Lys399=
NM_000526.5:c.1197G= MANE Select NP_000517.3:p.Lys399=
Search 100 bp 5'
Search 100 bp 3'