Canonical Allele Identifier: CA399478263
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584342T>A , CM000679.2:g.41584342T>A GRCh38
NC_000017.10:g.39740594T>A , CM000679.1:g.39740594T>A GRCh37
NC_000017.9:g.36994120T>A NCBI36
NG_008624.1:g.7554A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.680A>T MANE Select ENSP00000167586.6:p.Glu227Val
ENST00000167586.6:c.680A>T ENSP00000167586.6:p.Glu227Val
ENST00000476662.1:n.130A>T
NM_000526.4:c.680A>T NP_000517.2:p.Glu227Val
NM_000526.5:c.680A>T MANE Select NP_000517.3:p.Glu227Val