Canonical Allele Identifier: CA399474974
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583121A>T , CM000679.2:g.41583121A>T GRCh38
NC_000017.10:g.39739373A>T , CM000679.1:g.39739373A>T GRCh37
NC_000017.9:g.36992899A>T NCBI36
NG_008624.1:g.8775T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1294T>A MANE Select ENSP00000167586.6:p.Ser432Thr
ENST00000167586.6:c.1294T>A ENSP00000167586.6:p.Ser432Thr
ENST00000441550.2:n.241T>A
NM_000526.4:c.1294T>A NP_000517.2:p.Ser432Thr
NM_000526.5:c.1294T>A MANE Select NP_000517.3:p.Ser432Thr