Canonical Allele Identifier: CA399482697
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs748396111

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586507G>A , CM000679.2:g.41586507G>A GRCh38
NC_000017.10:g.39742759G>A , CM000679.1:g.39742759G>A GRCh37
NC_000017.9:g.36996285G>A NCBI36
NG_008624.1:g.5389C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.328C>T MANE Select ENSP00000167586.6:p.Leu110Phe
ENST00000167586.6:c.328C>T ENSP00000167586.6:p.Leu110Phe
NM_000526.4:c.328C>T NP_000517.2:p.Leu110Phe
NM_000526.5:c.328C>T MANE Select NP_000517.3:p.Leu110Phe