Canonical Allele Identifier: CA2260086993
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586720A= , CM000679.2:g.41586720A= GRCh38
NC_000017.10:g.39742972A= , CM000679.1:g.39742972A= GRCh37
NC_000017.9:g.36996498A= NCBI36
NG_008624.1:g.5176T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.115T= MANE Select ENSP00000167586.6:p.Ser39=
ENST00000167586.6:c.115T= ENSP00000167586.6:p.Ser39=
NM_000526.4:c.115T= NP_000517.2:p.Ser39=
NM_000526.5:c.115T= MANE Select NP_000517.3:p.Ser39=
Search 100 bp 5'
Search 100 bp 3'