Canonical Allele Identifier: CA399474992
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583125C>A , CM000679.2:g.41583125C>A GRCh38
NC_000017.10:g.39739377C>A , CM000679.1:g.39739377C>A GRCh37
NC_000017.9:g.36992903C>A NCBI36
NG_008624.1:g.8771G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1290G>T MANE Select ENSP00000167586.6:p.Gln430His
ENST00000167586.6:c.1290G>T ENSP00000167586.6:p.Gln430His
ENST00000441550.2:n.237G>T
NM_000526.4:c.1290G>T NP_000517.2:p.Gln430His
NM_000526.5:c.1290G>T MANE Select NP_000517.3:p.Gln430His