Canonical Allele Identifier: CA399478857
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584405G>A , CM000679.2:g.41584405G>A GRCh38
NC_000017.10:g.39740657G>A , CM000679.1:g.39740657G>A GRCh37
NC_000017.9:g.36994183G>A NCBI36
NG_008624.1:g.7491C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.617C>T MANE Select ENSP00000167586.6:p.Thr206Ile
ENST00000167586.6:c.617C>T ENSP00000167586.6:p.Thr206Ile
ENST00000476662.1:n.67C>T
NM_000526.4:c.617C>T NP_000517.2:p.Thr206Ile
NM_000526.5:c.617C>T MANE Select NP_000517.3:p.Thr206Ile