Canonical Allele Identifier: CA399477064
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583771A>C , CM000679.2:g.41583771A>C GRCh38
NC_000017.10:g.39740023A>C , CM000679.1:g.39740023A>C GRCh37
NC_000017.9:g.36993549A>C NCBI36
NG_008624.1:g.8125T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.916T>G MANE Select ENSP00000167586.6:p.Phe306Val
ENST00000167586.6:c.916T>G ENSP00000167586.6:p.Phe306Val
ENST00000476662.1:n.366T>G
NM_000526.4:c.916T>G NP_000517.2:p.Phe306Val
NM_000526.5:c.916T>G MANE Select NP_000517.3:p.Phe306Val