Canonical Allele Identifier: CA399477106
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583777C>T , CM000679.2:g.41583777C>T GRCh38
NC_000017.10:g.39740029C>T , CM000679.1:g.39740029C>T GRCh37
NC_000017.9:g.36993555C>T NCBI36
NG_008624.1:g.8119G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.910G>A MANE Select ENSP00000167586.6:p.Glu304Lys
ENST00000167586.6:c.910G>A ENSP00000167586.6:p.Glu304Lys
ENST00000476662.1:n.360G>A
NM_000526.4:c.910G>A NP_000517.2:p.Glu304Lys
NM_000526.5:c.910G>A MANE Select NP_000517.3:p.Glu304Lys