Canonical Allele Identifier: CA2260085573
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583803G= , CM000679.2:g.41583803G= GRCh38
NC_000017.10:g.39740055G= , CM000679.1:g.39740055G= GRCh37
NC_000017.9:g.36993581G= NCBI36
NG_008624.1:g.8093C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.884C= MANE Select ENSP00000167586.6:p.Ala295=
ENST00000167586.6:c.884C= ENSP00000167586.6:p.Ala295=
ENST00000476662.1:n.334C=
NM_000526.4:c.884C= NP_000517.2:p.Ala295=
NM_000526.5:c.884C= MANE Select NP_000517.3:p.Ala295=
Search 100 bp 5'
Search 100 bp 3'