Canonical Allele Identifier: CA399477639
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583882T>A , CM000679.2:g.41583882T>A GRCh38
NC_000017.10:g.39740134T>A , CM000679.1:g.39740134T>A GRCh37
NC_000017.9:g.36993660T>A NCBI36
NG_008624.1:g.8014A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.805A>T MANE Select ENSP00000167586.6:p.Asn269Tyr
ENST00000167586.6:c.805A>T ENSP00000167586.6:p.Asn269Tyr
ENST00000476662.1:n.255A>T
NM_000526.4:c.805A>T NP_000517.2:p.Asn269Tyr
NM_000526.5:c.805A>T MANE Select NP_000517.3:p.Asn269Tyr