Canonical Allele Identifier: CA399478411
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584363C>T , CM000679.2:g.41584363C>T GRCh38
NC_000017.10:g.39740615C>T , CM000679.1:g.39740615C>T GRCh37
NC_000017.9:g.36994141C>T NCBI36
NG_008624.1:g.7533G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.659G>A MANE Select ENSP00000167586.6:p.Gly220Asp
ENST00000167586.6:c.659G>A ENSP00000167586.6:p.Gly220Asp
ENST00000476662.1:n.109G>A
NM_000526.4:c.659G>A NP_000517.2:p.Gly220Asp
NM_000526.5:c.659G>A MANE Select NP_000517.3:p.Gly220Asp