Canonical Allele Identifier: CA2260085733
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584059C= , CM000679.2:g.41584059C= GRCh38
NC_000017.10:g.39740311C= , CM000679.1:g.39740311C= GRCh37
NC_000017.9:g.36993837C= NCBI36
NG_008624.1:g.7837G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-138G= MANE Select ENSP00000167586.6:n.766-138G=
ENST00000167586.6:c.766-138G= ENSP00000167586.6:n.766-138G=
ENST00000476662.1:n.216-138G=
NM_000526.4:c.766-138G= NP_000517.2:n.766-138G=
NM_000526.5:c.766-138G= MANE Select NP_000517.3:n.766-138G=