Canonical Allele Identifier: CA399475668
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583334T>G , CM000679.2:g.41583334T>G GRCh38
NC_000017.10:g.39739586T>G , CM000679.1:g.39739586T>G GRCh37
NC_000017.9:g.36993112T>G NCBI36
NG_008624.1:g.8562A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1175A>C MANE Select ENSP00000167586.6:p.Glu392Ala
ENST00000167586.6:c.1175A>C ENSP00000167586.6:p.Glu392Ala
ENST00000441550.2:n.122A>C
ENST00000476662.1:n.625A>C
NM_000526.4:c.1175A>C NP_000517.2:p.Glu392Ala
NM_000526.5:c.1175A>C MANE Select NP_000517.3:p.Glu392Ala