Canonical Allele Identifier: CA2260086020
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907465628
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584610del , CM000679.2:g.41584610del GRCh38
NC_000017.10:g.39740862del , CM000679.1:g.39740862del GRCh37
NC_000017.9:g.36994388del NCBI36
NG_008624.1:g.7286del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-197del MANE Select ENSP00000167586.6:n.609-197del
ENST00000167586.6:c.609-197del ENSP00000167586.6:n.609-197del
NM_000526.4:c.609-197del NP_000517.2:n.609-197del
NM_000526.5:c.609-197del MANE Select NP_000517.3:n.609-197del
Search 100 bp 5'
Search 100 bp 3'