Canonical Allele Identifier: CA216825
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66304
ClinVar RCV Id: RCV000056666
dbSNP Id: rs267607399

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583368C>T , CM000679.2:g.41583368C>T GRCh38
NC_000017.10:g.39739620C>T , CM000679.1:g.39739620C>T GRCh37
NC_000017.9:g.36993146C>T NCBI36
NG_008624.1:g.8528G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1141G>A MANE Select ENSP00000167586.6:p.Glu381Lys
ENST00000167586.6:c.1141G>A ENSP00000167586.6:p.Glu381Lys
ENST00000441550.2:n.88G>A
ENST00000476662.1:n.591G>A
NM_000526.4:c.1141G>A NP_000517.2:p.Glu381Lys
NM_000526.5:c.1141G>A MANE Select NP_000517.3:p.Glu381Lys