Canonical Allele Identifier: CA399478408
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907456023

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.659G>T MANE Select ENSP00000167586.6:p.Gly220Val
ENST00000167586.6:c.659G>T ENSP00000167586.6:p.Gly220Val
ENST00000476662.1:n.109G>T
NM_000526.4:c.659G>T NP_000517.2:p.Gly220Val
NM_000526.5:c.659G>T MANE Select NP_000517.3:p.Gly220Val