Canonical Allele Identifier: CA2260085444
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583525A= , CM000679.2:g.41583525A= GRCh38
NC_000017.10:g.39739777A= , CM000679.1:g.39739777A= GRCh37
NC_000017.9:g.36993303A= NCBI36
NG_008624.1:g.8371T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1053+26T= MANE Select ENSP00000167586.6:n.1053+26T=
ENST00000167586.6:c.1053+26T= ENSP00000167586.6:n.1053+26T=
ENST00000476662.1:n.503+26T=
NM_000526.4:c.1053+26T= NP_000517.2:n.1053+26T=
NM_000526.5:c.1053+26T= MANE Select NP_000517.3:n.1053+26T=