Canonical Allele Identifier: CA2260085843
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584211G= , CM000679.2:g.41584211G= GRCh38
NC_000017.10:g.39740463G= , CM000679.1:g.39740463G= GRCh37
NC_000017.9:g.36993989G= NCBI36
NG_008624.1:g.7685C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.765+46C= MANE Select ENSP00000167586.6:n.765+46C=
ENST00000167586.6:c.765+46C= ENSP00000167586.6:n.765+46C=
ENST00000476662.1:n.215+46C=
NM_000526.4:c.765+46C= NP_000517.2:n.765+46C=
NM_000526.5:c.765+46C= MANE Select NP_000517.3:n.765+46C=