Canonical Allele Identifier: CA399474918
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583109G>A , CM000679.2:g.41583109G>A GRCh38
NC_000017.10:g.39739361G>A , CM000679.1:g.39739361G>A GRCh37
NC_000017.9:g.36992887G>A NCBI36
NG_008624.1:g.8787C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1306C>T MANE Select ENSP00000167586.6:p.Gln436Ter
ENST00000167586.6:c.1306C>T ENSP00000167586.6:p.Gln436Ter
ENST00000441550.2:n.253C>T
NM_000526.4:c.1306C>T NP_000517.2:p.Gln436Ter
NM_000526.5:c.1306C>T MANE Select NP_000517.3:p.Gln436Ter