Canonical Allele Identifier: CA2260085569
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583788T= , CM000679.2:g.41583788T= GRCh38
NC_000017.10:g.39740040T= , CM000679.1:g.39740040T= GRCh37
NC_000017.9:g.36993566T= NCBI36
NG_008624.1:g.8108A=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.899A= MANE Select ENSP00000167586.6:p.Lys300=
ENST00000167586.6:c.899A= ENSP00000167586.6:p.Lys300=
ENST00000476662.1:n.349A=
NM_000526.4:c.899A= NP_000517.2:p.Lys300=
NM_000526.5:c.899A= MANE Select NP_000517.3:p.Lys300=