Canonical Allele Identifier: CA2576267698
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584442_41584443del , CM000679.2:g.41584442_41584443del GRCh38
NC_000017.10:g.39740694_39740695del , CM000679.1:g.39740694_39740695del GRCh37
NC_000017.9:g.36994220_36994221del NCBI36
NG_008624.1:g.7455_7456del

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-28_609-27del MANE Select ENSP00000167586.6:n.609-28_609-27del
ENST00000167586.6:c.609-28_609-27del ENSP00000167586.6:n.609-28_609-27del
ENST00000476662.1:n.31_32del
NM_000526.4:c.609-28_609-27del NP_000517.2:n.609-28_609-27del
NM_000526.5:c.609-28_609-27del MANE Select NP_000517.3:n.609-28_609-27del
Search 100 bp 5'
Search 100 bp 3'