Canonical Allele Identifier: CA8562435
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1221511
ClinVar RCV Id: RCV001597802
dbSNP Id: rs35380497

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583207dup , CM000679.2:g.41583207dup GRCh38
NC_000017.10:g.39739459dup , CM000679.1:g.39739459dup GRCh37
NC_000017.9:g.36992985dup NCBI36
NG_008624.1:g.8696dup

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1274+35dup MANE Select ENSP00000167586.6:n.1274+35dup
ENST00000167586.6:c.1274+35dup ENSP00000167586.6:n.1274+35dup
ENST00000441550.2:n.221+35dup
NM_000526.4:c.1274+35dup NP_000517.2:n.1274+35dup
NM_000526.5:c.1274+35dup MANE Select NP_000517.3:n.1274+35dup