Canonical Allele Identifier: CA399482063
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586381G>T , CM000679.2:g.41586381G>T GRCh38
NC_000017.10:g.39742633G>T , CM000679.1:g.39742633G>T GRCh37
NC_000017.9:g.36996159G>T NCBI36
NG_008624.1:g.5515C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.454C>A MANE Select ENSP00000167586.6:p.Gln152Lys
ENST00000167586.6:c.454C>A ENSP00000167586.6:p.Gln152Lys
NM_000526.4:c.454C>A NP_000517.2:p.Gln152Lys
NM_000526.5:c.454C>A MANE Select NP_000517.3:p.Gln152Lys