Canonical Allele Identifier: CA399484123
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586813A>T , CM000679.2:g.41586813A>T GRCh38
NC_000017.10:g.39743065A>T , CM000679.1:g.39743065A>T GRCh37
NC_000017.9:g.36996591A>T NCBI36
NG_008624.1:g.5083T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.22T>A MANE Select ENSP00000167586.6:p.Phe8Ile
ENST00000167586.6:c.22T>A ENSP00000167586.6:p.Phe8Ile
NM_000526.4:c.22T>A NP_000517.2:p.Phe8Ile
NM_000526.5:c.22T>A MANE Select NP_000517.3:p.Phe8Ile