Canonical Allele Identifier: CA2560357795
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583710_41583712del , CM000679.2:g.41583710_41583712del GRCh38
NC_000017.10:g.39739962_39739964del , CM000679.1:g.39739962_39739964del GRCh37
NC_000017.9:g.36993488_36993490del NCBI36
NG_008624.1:g.8184_8186del

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.928-36_928-34del MANE Select ENSP00000167586.6:n.928-36_928-34del
ENST00000167586.6:c.928-36_928-34del ENSP00000167586.6:n.928-36_928-34del
ENST00000476662.1:n.378-36_378-34del
NM_000526.4:c.928-36_928-34del NP_000517.2:n.928-36_928-34del
NM_000526.5:c.928-36_928-34del MANE Select NP_000517.3:n.928-36_928-34del