Canonical Allele Identifier: CA2637837934
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586859_41586861del , CM000679.2:g.41586859_41586861del GRCh38
NC_000017.10:g.39743111_39743113del , CM000679.1:g.39743111_39743113del GRCh37
NC_000017.9:g.36996637_36996639del NCBI36
NG_008624.1:g.5035_5037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-27_-25del MANE Select ENSP00000167586.6:n.-27_-25del
ENST00000167586.6:c.-27_-25del ENSP00000167586.6:n.-27_-25del
NM_000526.4:c.-27_-25del NP_000517.2:n.-27_-25del
NM_000526.5:c.-27_-25del MANE Select NP_000517.3:n.-27_-25del