Canonical Allele Identifier: CA2260085370
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583361T= , CM000679.2:g.41583361T= GRCh38
NC_000017.10:g.39739613T= , CM000679.1:g.39739613T= GRCh37
NC_000017.9:g.36993139T= NCBI36
NG_008624.1:g.8535A=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1148A= MANE Select ENSP00000167586.6:p.Gln383=
ENST00000167586.6:c.1148A= ENSP00000167586.6:p.Gln383=
ENST00000441550.2:n.95A=
ENST00000476662.1:n.598A=
NM_000526.4:c.1148A= NP_000517.2:p.Gln383=
NM_000526.5:c.1148A= MANE Select NP_000517.3:p.Gln383=