Canonical Allele Identifier: CA2260085372
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583368C= , CM000679.2:g.41583368C= GRCh38
NC_000017.10:g.39739620C= , CM000679.1:g.39739620C= GRCh37
NC_000017.9:g.36993146C= NCBI36
NG_008624.1:g.8528G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1141G= MANE Select ENSP00000167586.6:p.Glu381=
ENST00000167586.6:c.1141G= ENSP00000167586.6:p.Glu381=
ENST00000441550.2:n.88G=
ENST00000476662.1:n.591G=
NM_000526.4:c.1141G= NP_000517.2:p.Glu381=
NM_000526.5:c.1141G= MANE Select NP_000517.3:p.Glu381=