Canonical Allele Identifier: CA399484298
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586831T>A , CM000679.2:g.41586831T>A GRCh38
NC_000017.10:g.39743083T>A , CM000679.1:g.39743083T>A GRCh37
NC_000017.9:g.36996609T>A NCBI36
NG_008624.1:g.5065A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.4A>T MANE Select ENSP00000167586.6:p.Thr2Ser
ENST00000167586.6:c.4A>T ENSP00000167586.6:p.Thr2Ser
NM_000526.4:c.4A>T NP_000517.2:p.Thr2Ser
NM_000526.5:c.4A>T MANE Select NP_000517.3:p.Thr2Ser