Canonical Allele Identifier: CA2637834263
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583156del , CM000679.2:g.41583156del GRCh38
NC_000017.10:g.39739408del , CM000679.1:g.39739408del GRCh37
NC_000017.9:g.36992934del NCBI36
NG_008624.1:g.8743del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1275-13del MANE Select ENSP00000167586.6:n.1275-13del
ENST00000167586.6:c.1275-13del ENSP00000167586.6:n.1275-13del
ENST00000441550.2:n.222-13del
NM_000526.4:c.1275-13del NP_000517.2:n.1275-13del
NM_000526.5:c.1275-13del MANE Select NP_000517.3:n.1275-13del