Canonical Allele Identifier: CA2637836453
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584541del , CM000679.2:g.41584541del GRCh38
NC_000017.10:g.39740793del , CM000679.1:g.39740793del GRCh37
NC_000017.9:g.36994319del NCBI36
NG_008624.1:g.7358del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-125del MANE Select ENSP00000167586.6:n.609-125del
ENST00000167586.6:c.609-125del ENSP00000167586.6:n.609-125del
NM_000526.4:c.609-125del NP_000517.2:n.609-125del
NM_000526.5:c.609-125del MANE Select NP_000517.3:n.609-125del