Canonical Allele Identifier: CA2260085509
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583671C= , CM000679.2:g.41583671C= GRCh38
NC_000017.10:g.39739923C= , CM000679.1:g.39739923C= GRCh37
NC_000017.9:g.36993449C= NCBI36
NG_008624.1:g.8225G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.933G= MANE Select ENSP00000167586.6:p.Glu311=
ENST00000167586.6:c.933G= ENSP00000167586.6:p.Glu311=
ENST00000476662.1:n.383G=
NM_000526.4:c.933G= NP_000517.2:p.Glu311=
NM_000526.5:c.933G= MANE Select NP_000517.3:p.Glu311=
Search 100 bp 5'
Search 100 bp 3'