Canonical Allele Identifier: CA8562420
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600246
ClinVar RCV Id: RCV002132208
dbSNP Id: rs897428

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583159A>G , CM000679.2:g.41583159A>G GRCh38
NC_000017.10:g.39739411A>G , CM000679.1:g.39739411A>G GRCh37
NC_000017.9:g.36992937A>G NCBI36
NG_008624.1:g.8737T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1275-19T>C MANE Select ENSP00000167586.6:n.1275-19T>C
ENST00000167586.6:c.1275-19T>C ENSP00000167586.6:n.1275-19T>C
ENST00000441550.2:n.222-19T>C
NM_000526.4:c.1275-19T>C NP_000517.2:n.1275-19T>C
NM_000526.5:c.1275-19T>C MANE Select NP_000517.3:n.1275-19T>C