Canonical Allele Identifier: CA216939
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66357
ClinVar RCV Id: RCV000056728
dbSNP Id: rs61027685

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586438C>G , CM000679.2:g.41586438C>G GRCh38
NC_000017.10:g.39742690C>G , CM000679.1:g.39742690C>G GRCh37
NC_000017.9:g.36996216C>G NCBI36
NG_008624.1:g.5458G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.397G>C MANE Select ENSP00000167586.6:p.Val133Leu
ENST00000167586.6:c.397G>C ENSP00000167586.6:p.Val133Leu
NM_000526.4:c.397G>C NP_000517.2:p.Val133Leu
NM_000526.5:c.397G>C MANE Select NP_000517.3:p.Val133Leu