Canonical Allele Identifier: CA8562402
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs113794908

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583050G>A , CM000679.2:g.41583050G>A GRCh38
NC_000017.10:g.39739302G>A , CM000679.1:g.39739302G>A GRCh37
NC_000017.9:g.36992828G>A NCBI36
NG_008624.1:g.8846C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+44C>T MANE Select ENSP00000167586.6:n.1321+44C>T
ENST00000167586.6:c.1321+44C>T ENSP00000167586.6:n.1321+44C>T
ENST00000441550.2:n.312C>T
NM_000526.4:c.1321+44C>T NP_000517.2:n.1321+44C>T
NM_000526.5:c.1321+44C>T MANE Select NP_000517.3:n.1321+44C>T