Canonical Allele Identifier: CA16620405
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 421214
ClinVar RCV Id: RCV000487128
dbSNP Id: rs1064794983

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586482G>A , CM000679.2:g.41586482G>A GRCh38
NC_000017.10:g.39742734G>A , CM000679.1:g.39742734G>A GRCh37
NC_000017.9:g.36996260G>A NCBI36
NG_008624.1:g.5414C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.353C>T MANE Select ENSP00000167586.6:p.Thr118Ile
ENST00000167586.6:c.353C>T ENSP00000167586.6:p.Thr118Ile
NM_000526.4:c.353C>T NP_000517.2:p.Thr118Ile
NM_000526.5:c.353C>T MANE Select NP_000517.3:p.Thr118Ile