Canonical Allele Identifier: CA2260085564
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583773C= , CM000679.2:g.41583773C= GRCh38
NC_000017.10:g.39740025C= , CM000679.1:g.39740025C= GRCh37
NC_000017.9:g.36993551C= NCBI36
NG_008624.1:g.8123G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.914G= MANE Select ENSP00000167586.6:p.Trp305=
ENST00000167586.6:c.914G= ENSP00000167586.6:p.Trp305=
ENST00000476662.1:n.364G=
NM_000526.4:c.914G= NP_000517.2:p.Trp305=
NM_000526.5:c.914G= MANE Select NP_000517.3:p.Trp305=