Canonical Allele Identifier: CA2260085120
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41582980C= , CM000679.2:g.41582980C= GRCh38
NC_000017.10:g.39739232C= , CM000679.1:g.39739232C= GRCh37
NC_000017.9:g.36992758C= NCBI36
NG_008624.1:g.8916G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+114G= MANE Select ENSP00000167586.6:n.1321+114G=
ENST00000167586.6:c.1321+114G= ENSP00000167586.6:n.1321+114G=
ENST00000441550.2:n.382G=
NM_000526.4:c.1321+114G= NP_000517.2:n.1321+114G=
NM_000526.5:c.1321+114G= MANE Select NP_000517.3:n.1321+114G=